CLAW II ORTHOLOC 3DSiRecalls & reported problems across all models
Wright Medical Technology, Inc. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one CLAW II ORTHOLOC 3DSi model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 1
We found 2 models of CLAW II ORTHOLOC 3DSi by Wright Medical Technology, Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Sep 27, 2023 and Sep 27, 2023 — classified as 1 injury.
1 FDA recall record name at least one of these models by its device identifier, 1 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
CLAW II ORTHOLOC 3DSi 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.
- Feb 2, 2023Open, Classified
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contained 40241425, and vice versa.
Z-1170-2023 · Root cause: Employee error · Recall details · FDA record ↗
Most reported CLAW II ORTHOLOC 3DSi problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Implant Pain1
CLAW II ORTHOLOC 3DSi models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CLAW II ORTHOLOC 3DSi 40241425Screw, fixation, bone1 recall0 reports
- CLAW II ORTHOLOC 3DSi 40240220Screw, fixation, bone1 report
Recent CLAW II ORTHOLOC 3DSi adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 27, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY OF THE RIGHT ANKLE DUE TO PAINFUL HARDWARE. PATIENT HAS A LONG HISTORY OF RIGID FLATFOOT AND A VALGUS DEGENERATIVE TIBIOTALAR ARTHRITIS.
Patient problems: Implant Pain
MAUDE report 17824147 ↗
Other Wright Medical Technology, Inc. products
- INFINITY51 models · 733 reports · 3 recalls
- INBONE56 models · 365 reports · 4 recalls
- INFINITY ADAPTIS8 models · 219 reports
- ORTHOLOC 3Di23 models · 28 reports · 2 recalls
- INFINITY BIOFOAM 3D5 models · 118 reports
- INFINITY EVERLAST20 models · 111 reports
- EVOLVE14 models · 28 reports · 1 recall
- SWANSON12 models · 17 reports · 1 recall
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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