LinkSymphoKneeRecalls & reported problems across all models
WALDEMAR LINK GmbH & Co. KG · 117 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
11 open recalls name at least one LinkSymphoKnee model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 79
- Deaths reported
- 0
- Injuries reported
- 33
- Recalls
- 11
We found 117 models of LinkSymphoKnee by WALDEMAR LINK GmbH & Co. KG in the FDA's device registry (GUDID). Together they are named in 79 adverse event reports in the FDA's MAUDE database, received between Feb 24, 2023 and Sep 25, 2026 — classified as 33 injuries, 46 malfunctions.
The most frequently reported specific device problem is “Positioning Failure” (46 reports).
11 FDA recall records name at least one of these models by its device identifier, 11 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
LinkSymphoKnee 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 31, 2025Open, Classified
Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.
Z-2541-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Apr 3, 2025Open, Classified
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
Z-1702-2025 · Root cause: Nonconforming Material/Component · names 30 of these models · Recall details · FDA record ↗
- Apr 3, 2025Open, Classified
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
Z-1701-2025 · Root cause: Nonconforming Material/Component · names 12 of these models · Recall details · FDA record ↗
- Apr 3, 2025Open, Classified
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
Z-1700-2025 · Root cause: Nonconforming Material/Component · names 20 of these models · Recall details · FDA record ↗
- Apr 3, 2025Open, Classified
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
Z-1699-2025 · Root cause: Nonconforming Material/Component · names 20 of these models · Recall details · FDA record ↗
- Feb 14, 2025Open, Classified
A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.
Z-1374-2025 · Root cause: Labeling Change Control · Recall details · FDA record ↗
- Feb 14, 2025Open, Classified
A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.
Z-1373-2025 · Root cause: Labeling Change Control · Recall details · FDA record ↗
- Feb 14, 2025Open, Classified
A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.
Z-1372-2025 · Root cause: Labeling Change Control · Recall details · FDA record ↗
- Apr 25, 2023Open, Classified
Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left instead of Medial-Right/Lateral-Left).
Z-1674-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Dec 23, 2022Open, Classified
Fixation screw was inserted through the wrong side of the augment (distal to proximal, as opposed to proximal to distal, which is the correct orientation).
Z-2067-2023 · Root cause: Component change control · Recall details · FDA record ↗
- Dec 23, 2022Open, Classified
Fixation screw was inserted through the wrong side of the augment (distal to proximal, as opposed to proximal to distal, which is the correct orientation).
Z-2066-2023 · Root cause: Component change control · Recall details · FDA record ↗
Most reported LinkSymphoKnee problems
Device problems
- Positioning Failure46
- Naturally Worn14
- Positioning Problem5
- Component Misassembled4
- Detachment of Device or Device Component4
- Device Dislodged or Dislocated4
- Loosening of Implant Not Related to Bone-Ingrowth4
- Material Deformation3
Patient problems
- No Clinical Signs, Symptoms or Conditions49
- Insufficient Information12
- Failure of Implant8
- Pain8
- Joint Laxity6
- Swelling/ Edema3
- Implant Pain2
- Medical device site infection1
LinkSymphoKnee models
117 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- LinkSymphoKnee 880-307/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 recalls2 reports
- LinkSymphoKnee 880-307/21PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER2 recalls2 reports
- LinkSymphoKnee 880-325/13PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 recalls1 report
- LinkSymphoKnee 880-100/50PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall1 report
- LinkSymphoKnee 880-305/11PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall1 report
- LinkSymphoKnee 880-305/22PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall1 report
- LinkSymphoKnee 880-313/11PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall1 report
- LinkSymphoKnee 880-313/22PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall1 report
- LinkSymphoKnee 880-315/21PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall1 report
- LinkSymphoKnee 880-300/21PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-301/11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-301/21PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-303/11PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-303/12PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-303/21PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-303/22PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-305/12PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-305/21PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-307/12PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-307/22PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-309/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-309/12PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-309/21PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-309/22PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-310/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-310/21PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-311/21PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-311/11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-313/12PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-313/21PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-315/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-315/12PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-315/22PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-317/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-317/12PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-317/21PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-317/22PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-319/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-319/12PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-319/21PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-319/22PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-320/12PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-320/22PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-321/12PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-321/22PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-323/13PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-323/23PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-325/23PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-327/13PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-327/23PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-329/13PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-329/23PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-331/11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-331/12PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-331/13PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-331/21PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-331/22PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-331/23PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-333/11PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-333/12PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-333/13PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-333/21PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-333/22PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-333/23PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-335/11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-335/12PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-335/13PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-335/21PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-335/22PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-335/23PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-337/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-337/12PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-337/13PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-337/21PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-337/22PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-337/23PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-339/11PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-339/12PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-339/13PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-339/21PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-339/22PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-339/23PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-300/11PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-601/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-601/12PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-601/13PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 recall0 reports
- LinkSymphoKnee 880-201/10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER6 reports
- LinkSymphoKnee 880-203/10PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER5 reports
- LinkSymphoKnee 880-215/10PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER4 reports
- LinkSymphoKnee 880-217/10PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- LinkSymphoKnee 880-201/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- LinkSymphoKnee 880-213/12PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- LinkSymphoKnee 880-243/10PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- LinkSymphoKnee 880-253/12PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- LinkSymphoKnee 880-255/11PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- LinkSymphoKnee 880-241/10PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- LinkSymphoKnee 880-205/11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- LinkSymphoKnee 880-213/10PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- LinkSymphoKnee 880-213/11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- LinkSymphoKnee 880-217/11PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
Recent LinkSymphoKnee adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 25, 2026Material Erosion; Naturally Worn
worn plateau.
Patient problems: Metal Related Pathology; Pain; Swelling/ Edema
MAUDE report 50895364 ↗InjurySep 25, 2026Material Erosion; Naturally Worn
Infection, worn plateau and damaged femoral component.
Patient problems: Unspecified Infection
MAUDE report 50895343 ↗InjurySep 25, 2026Material Erosion; Naturally Worn
worn plateau and damaged femoral component.
Patient problems: Pain; Swelling/ Edema
MAUDE report 50895341 ↗InjuryAug 12, 2026Naturally Worn; Scratched Material
InjuryAug 4, 2026Naturally Worn
Patient problems: Pain
MAUDE report 50126490 ↗InjuryAug 4, 2026Naturally Worn
InjuryJul 27, 2026Naturally Worn
InjuryJul 10, 2026Naturally Worn; Loosening of Implant Not Related to Bone-Ingrowth
InjuryMay 19, 2026Naturally Worn
NOTIFIED ON 4/28/2026 REGARDING A REVISION TO AN LSK TIBIAL PLATEAU WITH DR. (B)(6) THAT OCCURRED ON (B)(6) 2026. THE ORIGINAL SURGERY WAS PERFORMED ON (B)(6) 2023. EXPLANTED PLATEAU WILL NOT BE RETURNED. [CUSTOMER].
Patient problems: Insufficient Information
MAUDE report 25215430 ↗InjuryMay 14, 2026Insufficient Device Problem Information
NOTIFIED ON (B)(6) 2026 REGARDING A REVISION TO AN LSK TIBIAL PLATEAU WITH DR. (B)(6) THAT OCCURRED ON (B)(6) 2026. THE ORIGINAL SURGERY WAS PERFORMED ON (B)(6) 2023.
Patient problems: Joint Laxity
MAUDE report 25175439 ↗InjuryMar 30, 2026Naturally Worn
InjuryMar 23, 2026Naturally Worn
InjuryMar 4, 2026Naturally Worn
InjuryFeb 26, 2026Naturally Worn
InjuryJan 5, 2026Material Deformation; Naturally Worn
Other WALDEMAR LINK GmbH & Co. KG products
- Unicondylar Sled Prosthesis48 models · 12 reports · 48 recalls
- Endo-Model Modular Knee Prosthesis System64 models · 57 reports · 12 recalls
- LINK Instrument14 models · 8 reports · 12 recalls
- Endo-Model SL Knee Prosthesis System25 models · 52 reports · 6 recalls
- Endo-Model Standard Knee Prosthesis System15 models · 19 reports · 6 recalls
- LINK Embrace Shoulder System Line Extension2 models · 1 reports · 4 recalls
- SPII Model Lubinus174 models · 6 reports · 3 recalls
- Endo-Model Knee System - Instruments5 models · 6 reports · 2 recalls
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.
How reports and recalls are matched · Editorial policy · Report an error on this page