Wright Medical Technology, Inc. 2023-03-08 Health serious FDA
Health · FDA · Recall #FDA-Z-1170-2023
ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device Recall
Issued March 8, 2023 · Wright Medical Technology, Inc.
In March 2023, Wright Medical Technology, Inc. recalled the ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Wright Medical Technology, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Wright Medical Technology, Inc.
- Category
- Health
- Recall date
- March 8, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the state of NY.
- Recall number
- FDA-Z-1170-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Wright Medical Technology, Inc. has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.