ScorpioRecalls & reported problems across all models

Howmedica Osteonics Corp. · 107 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

28 open recalls name at least one Scorpio model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports: 113
Deaths reported: 0
Injuries reported: 91
Recalls: 28

We found 107 models of Scorpio by Howmedica Osteonics Corp. in the FDA's device registry (GUDID). Together they are named in 113 adverse event reports in the FDA's MAUDE database, received between Jan 11, 2017 and Aug 24, 2026 — classified as 91 injuries, 22 malfunctions.

The most frequently reported specific device problem is “Fracture” (22 reports).

28 FDA recall records name at least one of these models by its device identifier, 28 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Reports received per month, all models

Last 36 months. The most recent month may be incomplete.

Scorpio recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

Jul 30, 2026Open, Classified
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.
Z-3206-2026 · Root cause: Process change control · names 7 of these models · Recall details · FDA record ↗
Jul 30, 2026Open, Classified
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.
Z-3197-2026 · Root cause: Process change control · names 15 of these models · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0900-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0899-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0898-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0897-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0896-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0895-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0894-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0893-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0892-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0891-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0890-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0889-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0888-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0887-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0886-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0885-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0884-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0883-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0882-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0881-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0880-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0879-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0878-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0877-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0876-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Dec 1, 2023Open, Classified
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Z-0875-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

Most reported Scorpio problems

Device problems

Fracture22
Unstable22
Adverse Event Without Identified Device or Use Problem17
Insufficient Device Problem Information17
Material Discolored11
Naturally Worn9
Osseointegration Problem6
Break5

Patient problems

Injury50
Pain16
Unspecified Infection15
Insufficient Information11
No Clinical Signs, Symptoms or Conditions11
Ambulation or Postural Difficulties10
No Consequences Or Impact To Patient9
Inadequate Osseointegration8

Scorpio models

107 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.

Scorpio 73-2710
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
3 recalls0 reports
Scorpio 73-3910
PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
2 recalls4 reports
Scorpio 73-3508
PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
2 recalls3 reports
Scorpio 73-3708
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 recalls3 reports
Scorpio 73-2910
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 recalls1 report
Scorpio 73-3710
PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER
2 recalls1 report
Scorpio 73-0910
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 recalls1 report
Scorpio 73-3110
PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER
2 recalls0 reports
Scorpio 73-0110
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 recalls0 reports
Scorpio 73-0710
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 recalls0 reports
Scorpio 82-2-0910
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall3 reports
Scorpio 82-2-0908
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall1 report
Scorpio 72-16-0910
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall1 report
Scorpio 82-3-0318
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 82-2-0512
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 82-2-0518
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 82-2-0912
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-15-0324
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-16-0512
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-16-0518
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-16-0908
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-16-0912
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-16-1112
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 73-2610
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 73-2110
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 73-3308
PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
1 recall0 reports
Scorpio 72-4-0321
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-0324
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-0510
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-7512
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-7516
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-7518
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-7514
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-7521
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-7524
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 72-4-9114
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 73-0510
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 recall0 reports
Scorpio 82-7-0510
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
5 reports
Scorpio 82-7-0708
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
5 reports
Scorpio 82-3-0918
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
4 reports
Scorpio 72-25-1110
PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
3 reports
Scorpio 82-6-0710
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
3 reports
Scorpio 82-3-0310
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 82-3-0512
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 82-3-0910
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 82-2-0710
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 72-15-0710
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 77-4005
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 72-25-1112
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 82-6-0908
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 82-7-0508
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 82-7-0908
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
2 reports
Scorpio 82-3-0312
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-3-0508
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-3-0510
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-3-0515
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-3-0715
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-2-0708
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-2-1110
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-13-0908
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-13-0915
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-13-0921
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-13-0712
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-15-0510
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-15-0908
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-16-0715
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 73-20-0510
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 73-20-3508
PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
1 report
Scorpio 70-3011L
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 70-3011R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 70-4107R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 70-4113R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 71-4509L
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 76-4013L
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 76-4105R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 76-4109R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 81-4405R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-25-0912
PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-26-0710
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 80-4405R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 80-4409L
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 80-4409R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 80-4408R
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-6-0510
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-6-0508
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-6-0512
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-6-0912
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-6-1110
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-0312
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-0308
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-0315
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-0512
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-0710
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-0712
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-0910
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-0912
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-1110
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 82-7-1115
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-4-0316
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report
Scorpio 72-4-0521
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
1 report

Recent Scorpio adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

InjuryAug 24, 2026Unstable
The patient had an Index Left TKA on (b)(6) 2013. The patient developed instability and hyperextension, and was revised on (b)(6) 2025. All components exchanged, except the Patella.
Patient problems: Joint Laxity
MAUDE report 50418425 ↗
InjuryJan 23, 2026Adverse Event Without Identified Device or Use Problem
THE FOLLOWING INFORMATION WAS PROVIDED: RIGHT TOTAL KNEE WASH OUT / POLY SWAP DUE TO INFECTION TREATMENT.
Patient problems: Unspecified Infection
MAUDE report 24159506 ↗
InjuryOct 21, 2025Fracture; Fracture
THE FOLLOWING INFORMATION WAS PROVIDED: THIS PI IS FOR THE 2025 REVISION. AS PER PSS IMPLANT REQUEST CASE (B)(4): FAILED RIGHT KNEE TOTAL KNEE WITH BROKEN COMPONENTS; MORBID OBESITY WITH BMI GREATER THAN 44. THIS PATIENT HAS A # 9 SCORPIO TS FEMORAL COMPONENT WITH A 23X80 STEM EXTENDER. THERE IS A FRACTURE OF THE IMPLANT AT THE STEM FEMORAL JUNCTION. THE PATIENT HAS A #13 SCORPIO TIBIAL TRAY WITH 10MM AUGMENTS MEDIAL AND LATERAL AND A 16X80 STEM EXTENDER. ALSO IMPLANTED IN TIBIA IS A 59MM TRABECULAR METAL CONE (ZIMMER). CURRENTLY A SIZE 11 8MM SCORPIO PS TIBIAL BEARING IS IMPLANTED. NEEDED FOR THIS NEXT REVISION IS AN INSERT (PS OR TS) TO MATE WITH A TRIATHLON TS FEMORAL COMPONENT. THE SURGEON NEED TO LEAVE THE CURRENT TIBIAL CONSTRUCT IMPLANTED. PATIENT HAS HAD SEVERAL KNEE REVISIONS. 2005 BOTH COMPONENTS REVISED, 2006 TIBIAL INSERT REVISED, 2014 THE TIBIAL TRAY AND INSERT REVISED.
Patient problems: Insufficient Information
MAUDE report 23346346 ↗
InjuryOct 7, 2024Fracture; Adverse Event Without Identified Device or Use Problem; Fracture; Adverse Event Without Identified Device or Use Problem
SUBJECT HAD A LEFT TKA ON (B)(6) 2004. ON (B)(6) 2004 PATIENT FELL OFF A LADDER SUSTAINING A SUPRACONDYLAR FEMUR FRACTURE. AN ORIF WITH COMPETITOR COMPONENTS WAS PERFORMED, NO IMPLANTS WERE REMOVED.
Patient problems: Fall; Fibrosis; Insufficient Information; Loss of Range of Motion
MAUDE report 20381876 ↗
InjuryApr 29, 2024Unstable; Unstable
LEFT TOTAL KNEE TIBIAL BEARING POLY SWAP DUE TO INSTABILITY.
Patient problems: Insufficient Information
MAUDE report 19201260 ↗
InjuryMar 20, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT HAD AN INFECTION. AND UNDERWENT A BILATERAL REVISION.
Patient problems: Unspecified Infection
MAUDE report 18941601 ↗
InjuryJan 12, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED BY THE SALE REP THAT PATIENT NEEDS A REVISION SURGERY DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 18500409 ↗
MalfunctionNov 8, 2023Material Discolored; Material Discolored
73-3708 LOT JR5N CAME OUT OF THE BOX YELLOW
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18097331 ↗
MalfunctionNov 8, 2023Material Discolored; Material Discolored
73-3708 LOT JR5N CAME OUT OF THE BOX YELLOW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18097330 ↗
MalfunctionNov 8, 2023Material Discolored; Material Discolored
73-3910 LOT 4873 CAME OUT OF THE BOX YELLOW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18097225 ↗
MalfunctionNov 8, 2023Material Discolored; Material Discolored
73-3910 LOT 4873 CAME OUT OF THE BOX YELLOW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18097171 ↗
MalfunctionNov 8, 2023Material Discolored; Material Discolored
73-3910 LOT 4873 CAME OUT OF THE BOX YELLOW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18097167 ↗
MalfunctionNov 8, 2023Material Discolored; Material Discolored
73-3910 LOT 4873 CAME OUT OF THE BOX YELLOW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18097166 ↗
MalfunctionNov 8, 2023Material Discolored; Material Discolored
OPENED STERILE PACKAGED SCORPIO UNIVERSAL PATELLA AND PRODUCT WAS SLIGHTLY DISCOLORED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18096796 ↗
MalfunctionNov 8, 2023Material Discolored; Material Discolored
IMPLANT REFERENCE NUMBER 73-3508 WITH LOT NUMBERS 53TI AND Y7X2 HAD A YELLOW RING AROUND THE DIAMETER OF THE PATELLA IMPLANT WHEN OPENED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18096795 ↗

Other Howmedica Osteonics Corp. products

All Howmedica Osteonics Corp. devices →

Sources and updates

Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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