RECLAIMRecalls & reported problems across all models
Depuy (Ireland) · 149 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,328
- Deaths reported
- 0
- Injuries reported
- 281
- Recalls
- 0
We found 149 models of RECLAIM by Depuy (Ireland) in the FDA's device registry (GUDID). Together they are named in 1,328 adverse event reports in the FDA's MAUDE database, received between Jan 9, 2017 and Sep 22, 2026 — classified as 281 injuries, 1,047 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (313 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 RECLAIM problems
Device problems
- Device-Device Incompatibility313
- Break295
- Adverse Event Without Identified Device or Use Problem157
- Naturally Worn118
- Material Deformation102
- Material Twisted/Bent98
- Appropriate Device Problem Term/Code Not Available68
- Mechanical Jam68
Patient problems
- No Clinical Signs, Symptoms or Conditions518
- No Consequences Or Impact To Patient336
- Insufficient Information126
- No Code Available121
- Unspecified Infection104
- Inadequate Osseointegration69
- No Information62
- Not Applicable51
RECLAIM models
149 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- RECLAIM 2975-00-635EXTRACTOR157 reports
- RECLAIM 2975-31-040TEMPLATE90 reports
- RECLAIM 2975-31-045TEMPLATE80 reports
- RECLAIM 2975-00-800DRIVER, PROSTHESIS65 reports
- RECLAIM 2975-00-715ORTHOPEDIC MANUAL SURGICAL INSTRUMENT62 reports
- RECLAIM 2975-00-400DRIVER, PROSTHESIS61 reports
- RECLAIM 2975-00-300WRENCH51 reports
- RECLAIM 1975-20-075Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented41 reports
- RECLAIM 2975-29-075TEMPLATE38 reports
- RECLAIM 2975-29-085TEMPLATE36 reports
- RECLAIM 2975-00-720ORTHOPEDIC MANUAL SURGICAL INSTRUMENT33 reports
- RECLAIM 1975-24-085Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented29 reports
- RECLAIM 2975-00-500REAMER27 reports
- RECLAIM 2975-00-700ORTHOPEDIC MANUAL SURGICAL INSTRUMENT26 reports
- RECLAIM 1975-20-085Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented25 reports
- RECLAIM 2975-00-600ORTHOPEDIC MANUAL SURGICAL INSTRUMENT25 reports
- RECLAIM 2975-00-610ORTHOPEDIC MANUAL SURGICAL INSTRUMENT23 reports
- RECLAIM 2975-00-605ORTHOPEDIC MANUAL SURGICAL INSTRUMENT19 reports
- RECLAIM 1975-24-075Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented18 reports
- RECLAIM 2975-00-710ORTHOPEDIC MANUAL SURGICAL INSTRUMENT15 reports
- RECLAIM 1975-24-095Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented13 reports
- RECLAIM 2975-00-100TEMPLATE13 reports
- RECLAIM 1976-16-140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented11 reports
- RECLAIM 1976-18-140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented11 reports
- RECLAIM 2975-31-000SCREWDRIVER11 reports
- RECLAIM 1976-14-140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented10 reports
- RECLAIM 2975-00-725ORTHOPEDIC MANUAL SURGICAL INSTRUMENT9 reports
- RECLAIM 40-00000-30DRIVER, PROSTHESIS9 reports
- RECLAIM 1976-21-140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented8 reports
- RECLAIM 2975-00-510ORTHOPEDIC MANUAL SURGICAL INSTRUMENT8 reports
- RECLAIM 2975-00-615ORTHOPEDIC MANUAL SURGICAL INSTRUMENT8 reports
- RECLAIM 2975-00-910ORTHOPEDIC MANUAL SURGICAL INSTRUMENT8 reports
- RECLAIM 2976-14-140REAMER8 reports
- RECLAIM 1976-17-140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented7 reports
- RECLAIM 1976-20-140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented7 reports
- RECLAIM 2975-29-095TEMPLATE7 reports
- RECLAIM 1975-24-105Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented6 reports
- RECLAIM 1976-15-140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented6 reports
- RECLAIM 1977-18-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented6 reports
- RECLAIM 2975-00-735ORTHOPEDIC MANUAL SURGICAL INSTRUMENT6 reports
- RECLAIM 1976-16-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented5 reports
- RECLAIM 1976-19-140Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented5 reports
- RECLAIM 1977-22-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented5 reports
- RECLAIM 2975-00-620ORTHOPEDIC MANUAL SURGICAL INSTRUMENT5 reports
- 5 reports
- RECLAIM 2975-00-745ORTHOPEDIC MANUAL SURGICAL INSTRUMENT5 reports
- RECLAIM 2975-00-900ORTHOPEDIC MANUAL SURGICAL INSTRUMENT5 reports
- RECLAIM 2975-29-105TEMPLATE5 reports
- RECLAIM 2976-20-000REAMER5 reports
- RECLAIM 44-00000-40TEMPLATE5 reports
- RECLAIM 44-00000-45TEMPLATE5 reports
- RECLAIM 1975-20-095Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- RECLAIM 1975-20-105Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- RECLAIM 1975-28-075Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- RECLAIM 1976-18-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- RECLAIM 1977-14-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- RECLAIM 2975-00-505REAMER4 reports
- RECLAIM 2976-16-140REAMER4 reports
- RECLAIM 2976-17-140REAMER4 reports
- RECLAIM 2976-18-140REAMER4 reports
- RECLAIM 2976-19-140REAMER4 reports
- RECLAIM 1975-28-085Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented3 reports
- RECLAIM 1976-17-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented3 reports
- RECLAIM 1977-15-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented3 reports
- RECLAIM 1977-24-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented3 reports
- RECLAIM 2975-20-105REAMER3 reports
- RECLAIM 2975-31-105DRIVER, PROSTHESIS3 reports
- RECLAIM 2976-13-000REAMER3 reports
- RECLAIM 2976-15-140REAMER3 reports
- RECLAIM 2976-20-140REAMER3 reports
- RECLAIM 34-185-0014REAMER3 reports
- RECLAIM 34-185-0016REAMER3 reports
- RECLAIM 34-185-0019REAMER3 reports
- RECLAIM 34-185-0020REAMER3 reports
- RECLAIM 34-00000-00Orthopedic manual surgical instrument3 reports
- RECLAIM 44-00000-32REAMER3 reports
- RECLAIM 1975-28-095Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1976-14-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1976-21-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1977-16-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1977-16-240Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1977-19-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1977-20-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1977-20-240Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1977-21-190Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 1977-21-240Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 2975-00-200GAUGE, DEPTH2 reports
- RECLAIM 2975-00-760ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- RECLAIM 2975-00-770ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- RECLAIM 2975-28-105REAMER2 reports
- RECLAIM 2976-21-240REAMER2 reports
- RECLAIM 2976-22-190REAMER2 reports
- RECLAIM 2976-22-240REAMER2 reports
- RECLAIM 2976-27-190REAMER2 reports
- RECLAIM 2976-27-240REAMER2 reports
- RECLAIM 2976-50-050TRAY, SURGICAL, INSTRUMENT2 reports
- RECLAIM 10-235-4016Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- RECLAIM 44-00000-31IMPACTOR2 reports
- RECLAIM 1975-00-075Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- RECLAIM 1975-00-085Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
Recent RECLAIM adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026No Apparent Adverse Event
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50856910 ↗MalfunctionSep 22, 2026No Apparent Adverse Event
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50856909 ↗MalfunctionSep 11, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50740513 ↗MalfunctionAug 27, 2026Material Deformation
It was reported that instruments were rounded.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50484053 ↗MalfunctionAug 27, 2026Material Deformation
It was reported that instruments were rounded.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50484046 ↗MalfunctionAug 11, 2026Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50214351 ↗MalfunctionJul 29, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50074674 ↗MalfunctionJun 17, 2026Device-Device Incompatibility
IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE IT WAS OBSERVED THAT THE INSERTER WOULD NOT HOLD THE STEM FLUSH TO THE INSERTION HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25534075 ↗MalfunctionJun 16, 2026Material Deformation
IT WAS REPORTED THAT THREADS ARE STRIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25519839 ↗MalfunctionMay 26, 2026Break
IT WAS FOUND OUT THAT THE DEVICE WAS BROKEN WHEN CHECKING THE TRAY BEFORE GOING OUT TO SURGERY. IT DID NOT HAPPENED IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25277637 ↗MalfunctionMay 19, 2026Device-Device Incompatibility
IT WAS REPORTED THAT THE RECLAIM DISASSEMBLY BODY DEVICE AND THE DISASSEMBLY BODY COLLET DEVICE WERE FOUND STUCK TOGETHER AND WOULD NOT SEPARATE. THE EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT OR USER HARM AND NO DELAYS IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25222661 ↗MalfunctionMay 19, 2026Device-Device Incompatibility
IT WAS REPORTED THAT THE RECLAIM DISASSEMBLY BODY DEVICE AND THE DISASSEMBLY BODY COLLET DEVICE WERE FOUND STUCK TOGETHER AND WOULD NOT SEPARATE. THE EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT OR USER HARM AND NO DELAYS IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25222659 ↗MalfunctionMay 13, 2026Material Deformation
IT WAS REPORTED THAT THE ROD FOR MODULAR RECLAIM DISASSEMBLY IS BENT. IT DID NOT HAPPENED IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25161261 ↗MalfunctionMay 12, 2026Device-Device Incompatibility
IT WAS REPORTED THAT INSTRUMENTS BROKE DURING EXPLANT. THE PROXIMAL BODY OF RECLAIM WAS COLD WELDED ONTO THE DISTAL STEM. THE DISTAL STEM DID NOT COME OUT. PATIENT WAS NOT HARMED. NO DELAY IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25148567 ↗MalfunctionMay 12, 2026Device-Device Incompatibility
IT WAS REPORTED THAT INSTRUMENTS BROKE DURING EXPLANT. THE PROXIMAL BODY OF RECLAIM WAS COLD WELDED ONTO THE DISTAL STEM. THE DISTAL STEM DID NOT COME OUT. PATIENT WAS NOT HARMED. NO DELAY IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25148566 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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