Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific); Catalog Number: C-MM100434-00;
Recall
- Recall Number
- Z-2732-2024
- Event Number
- 95114
- Firm
- Howmedica Osteonics Corp.
- FEI Number
- 3003070421
- Product Code
- JDI
- Status
- Open, Classified
- Root Cause
- Process control
- Initiated
- August 5, 2024
- Posted
- August 26, 2024
- Address
- 325 Corporate Dr, Mahwah, NJ, 07430-2006
Description
Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific); Catalog Number: C-MM100434-00;
A patient specific, custom-made device was supplied for a surgical procedure that did not match the design proposal.
On August 5, 2024 an URGENT MEDICAL DEVICE RECALL letter was sent to their consignee. Actions Needed: Our records indicate that you have received the affected product, and that product has already been returned to Stryker. We therefore request that you read this notice carefully and complete the following actions. 1. Complete and sign the enclosed Urgent Medical Device Recall Business Reply Form. Please assist us in meeting our regulatory obligation by emailing back the attached Urgent Medical Device Recall Business Reply Form within 5 days. We regret any inconvenience this action may cause. For questions pertaining to the recall, please email [email protected]
International distribution to the country of Australia.
1 unit (OUS only)