Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific); Catalog Number: C-MM100
FDA device recall Z-2732-2024 · posted 2024-08-26 · Open, Classified
Recall details
- Recalling firm
- Howmedica Osteonics Corp.
- Reason for recall
- A patient specific, custom-made device was supplied for a surgical procedure that did not match the design proposal.
- Action taken
- 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 SO_M_PRODUCT_FIELD_ACTION_RESPONSE@stryker.com
- Root cause
- Process control
- Status
- Open, Classified
- Product code
- JDI
- Quantity affected
- 1 unit (OUS only)
- Distribution
- International distribution to the country of Australia.
- Date initiated
- 2024-08-05
- Date posted
- 2024-08-26
- Location
- Mahwah, NJ
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee (K222056) | Howmedica Osteonics Corp., Dba Stryker Orthopaedics | 2023-01-26 |
| GLOBAL MODULAR REPLACEMENT SYSTEM (GMRS) (K023087) | Howmedica Osteonics Corp. | 2002-12-16 |