LPSRecalls & reported problems across all models
Depuy (Ireland) · 113 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,152
- Deaths reported
- 0
- Injuries reported
- 1,022
- Recalls
- 0
We found 113 models of LPS by Depuy (Ireland) in the FDA's device registry (GUDID). Together they are named in 1,152 adverse event reports in the FDA's MAUDE database, received between Jun 22, 2017 and Sep 30, 2026 — classified as 1,022 injuries, 130 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (84 reports).
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
Most reported LPS problems
Device problems
- Adverse Event Without Identified Device or Use Problem708
- Device Dislodged or Dislocated84
- Insufficient Device Problem Information66
- Loss of or Failure to Bond46
- Fracture40
- Break38
- Device-Device Incompatibility35
- Loss of Osseointegration27
Patient problems
- Unspecified Infection401
- No Code Available272
- Pain214
- No Clinical Signs, Symptoms or Conditions81
- Joint Laxity65
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available63
- Insufficient Information61
- Joint Dislocation58
LPS models
113 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- LPS 1987-14-111PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER87 reports
- LPS 1987-15-000PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER82 reports
- LPS 1987-13-111Prosthesis, hip, semi-constrained, metal/polymer, cemented71 reports
- LPS 2987-72-030EXTRACTOR68 reports
- LPS 1987-14-105Prosthesis, hip, semi-constrained, metal/polymer, cemented57 reports
- LPS 1987-07-025Prosthesis, hip, semi-constrained, metal/polymer, cemented52 reports
- LPS 1987-27-012PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER46 reports
- LPS 1987-27-112PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER35 reports
- LPS 1987-13-105PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER34 reports
- LPS 1987-27-118PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER26 reports
- LPS 1987-07-035PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER24 reports
- LPS 1987-07-030Prosthesis, hip, semi-constrained, metal/polymer, cemented23 reports
- LPS 1987-07-045PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER21 reports
- LPS 1987-27-014PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER21 reports
- LPS 1987-09-055PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER20 reports
- LPS 1987-27-114PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER20 reports
- LPS 1987-27-116PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER18 reports
- LPS 1987-27-018PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER17 reports
- LPS 1987-27-121PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER17 reports
- LPS 1987-07-040Prosthesis, hip, semi-constrained, metal/polymer, cemented15 reports
- LPS 1987-07-065PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER15 reports
- LPS 1987-25-109PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER14 reports
- LPS 1987-27-123PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER13 reports
- LPS 1987-27-212PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER13 reports
- LPS 1987-10-105PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER12 reports
- LPS 1987-25-110PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER12 reports
- LPS 1987-07-085PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER11 reports
- LPS 1987-25-412PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER11 reports
- LPS 1987-27-016PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER10 reports
- LPS 1987-27-021PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER10 reports
- LPS 1987-27-023PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER10 reports
- LPS 1987-27-126PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER10 reports
- LPS 1987-07-105PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER8 reports
- LPS 1987-08-055Prosthesis, hip, semi-constrained, metal/polymer, cemented8 reports
- LPS 1987-25-413PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER7 reports
- LPS 1987-26-414PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER7 reports
- LPS 1987-27-128PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER7 reports
- LPS 1987-27-312PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER7 reports
- LPS 2987-72-045EXTRACTOR7 reports
- LPS 1987-07-125Prosthesis, hip, semi-constrained, metal/polymer, cemented6 reports
- LPS 1987-15-211PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER6 reports
- LPS 1987-25-111PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER6 reports
- LPS 1987-25-415PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER6 reports
- LPS 1987-27-131PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER6 reports
- LPS 1987-27-216PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER6 reports
- LPS 1987-27-321PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER6 reports
- LPS 2987-70-003IMPACTOR6 reports
- LPS 1987-12-105Prosthesis, hip, semi-constrained, metal/polymer, cemented5 reports
- LPS 1987-17-000PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER5 reports
- LPS 1987-21-105PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER5 reports
- LPS 1987-25-112Prosthesis, hip, semi-constrained, metal/polymer, cemented5 reports
- LPS 1987-27-231PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER5 reports
- LPS 1987-27-323PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER5 reports
- LPS 2987-70-001Bone mill5 reports
- LPS 1987-16-315Prosthesis, hip, semi-constrained, metal/polymer, cemented4 reports
- LPS 1987-26-412Prosthesis, hip, semi-constrained, metal/polymer, cemented4 reports
- LPS 1987-26-415PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER4 reports
- LPS 1987-26-416PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER4 reports
- LPS 1987-27-214PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- LPS 1987-27-218PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- LPS 1987-27-221PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- LPS 1987-27-316PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- LPS 1987-27-318PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- LPS 1987-27-326PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- LPS 2987-14-105ORTHOPEDIC MANUAL SURGICAL INSTRUMENT4 reports
- LPS 1987-11-105Prosthesis, hip, semi-constrained, metal/polymer, cemented3 reports
- LPS 1987-11-205Prosthesis, hip, semi-constrained, metal/polymer, cemented3 reports
- LPS 1987-16-215Prosthesis, hip, semi-constrained, metal/polymer, cemented3 reports
- LPS 1987-26-417Prosthesis, hip, semi-constrained, metal/polymer, cemented3 reports
- LPS 1987-27-223PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- LPS 1987-27-226PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- LPS 2987-72-035IMPACTOR3 reports
- LPS 1987-12-205Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- LPS 1987-15-212PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-15-214PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-15-313PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-15-315PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-16-212PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-16-214PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-16-217PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-16-317PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-26-109Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- LPS 1987-26-110PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER2 reports
- LPS 1987-26-111Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- LPS 1987-27-314PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- LPS 1987-27-328PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- LPS 2987-15-000TEMPLATE2 reports
- LPS 2987-40-040TEMPLATE2 reports
- LPS 2987-99-039TRAY, SURGICAL, INSTRUMENT2 reports
- LPS 1987-15-213Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- LPS 1987-15-215PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- LPS 1987-15-217PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- LPS 1987-15-311Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- LPS 1987-16-213PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- LPS 1987-16-216PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- LPS 1987-25-414Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- LPS 1987-25-416Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- LPS 1987-26-112PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- LPS 1987-26-413PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- LPS 1987-27-331PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
Recent LPS adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Device Dislodged or Dislocated
Patient problems: Joint Dislocation
MAUDE report 50951663 ↗InjurySep 23, 2026Adverse Event Without Identified Device or Use Problem
It was reported that Patients presents in the ER with pain. Exam suggests movement of the static spacer utilizing LPS components. In the OR, there is movement between the taper from the femoral sleeve adapter and the LPS segment. Existing modular components were removed. Tapers were thoroughly cleaned and dried and new components were placed successfully with no delay nor patient harm. No visible damage was found.DOI (b)(6) 2026.DOR (b)(6) 2026.Affected side-Right.
Patient problems: Pain
MAUDE report 50872021 ↗InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient presents with well fixed and positioned implants post full patellar allograft placement due to quadriceps rupture after revision TKA. Graft is incorporated and patella is in an appropriate position, however the proximal portion of the allograft has become lax. A longer segment is utilized to increase tension and patellar tracking is quite good. A shortening of the proximal tissues is performed and reinforced. A long leg cast is placed to protect the repair post operatively. No allegation is made against the components. No delay nor patient harm is noted. When removing the segment to lengthen the construct, the adapter was removed from the sleeve. There is no record of this device in optimize so not lot information is available.DOI: (b)(6) 2025.DOR: (b)(6) 2026.Affected Side: Right.
Patient problems: Joint Laxity; Unspecified Tissue Injury
MAUDE report 50788543 ↗InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient presents with well fixed and positioned implants post full patellar allograft placement due to quadriceps rupture after revision TKA. Graft is incorporated and patella is in an appropriate position, however the proximal portion of the allograft has become lax. A longer segment is utilized to increase tension and patellar tracking is quite good. A shortening of the proximal tissues is performed and reinforced. A long leg cast is placed to protect the repair post operatively. No allegation is made against the components. No delay nor patient harm is noted. When removing the segment to lengthen the construct, the adapter was removed from the sleeve. There is no record of this device in optimize so not lot information is available.DOI: (b)(6)2025.DOR: (b)(6)2026.Affected Side: Right.
Patient problems: Joint Laxity; Unspecified Tissue Injury
MAUDE report 50788380 ↗InjurySep 1, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient was revised due to fracture.DOI: Unknown,DOR: (b)(6) 2026,Affected side: Left Knee.
Patient problems: Bone Fracture(s)
MAUDE report 50544144 ↗InjurySep 1, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient was revised due to fracture.DOI: UnknownDOR: (b)(6), 2026Affected side: Left Knee.
Patient problems: Bone Fracture(s)
MAUDE report 50544114 ↗InjurySep 1, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient was revised due to fracture.DOI: Unknown,DOR: (b)(6), 2026,Affected side: Left Knee.
Patient problems: Bone Fracture(s)
MAUDE report 50543996 ↗MalfunctionAug 26, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50452686 ↗MalfunctionAug 26, 2026Break
It was reported that the device was checked after a case, and the spring/button was missing. There was no patient or user harm. There was no significant delay.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50452685 ↗InjuryAug 4, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient was draining and surgeon elected to wash out and change components.DOI: (b)(6)2026,DOR: (b)(6)2026,Affected Side: Right.
Patient problems: Fluid Discharge
MAUDE report 50129661 ↗InjuryAug 4, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient was draining and surgeon elected to wash out and change components.DOI: (b)(6) 2026.DOR: (b)(6) 2026.Affected Side: Right.
Patient problems: Fluid Discharge
MAUDE report 50129660 ↗MalfunctionAug 4, 2026Break; Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50126813 ↗InjuryAug 3, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient experienced pain.Affected side: Left knee.
Patient problems: Pain
MAUDE report 50116767 ↗InjuryJul 27, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient was revised due to pain.DOI: UnknownDOR: 07-06-2026Affected Side: Right
Patient problems: Pain
MAUDE report 50045654 ↗InjuryJul 27, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient was revised due to pain.DOI: Unknown,DOR: on (b)(6) 2026,Affected Side: Right.
Patient problems: Pain
MAUDE report 50045610 ↗
Other Depuy (Ireland) products
All Depuy (Ireland) 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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