Depuy P.F.C. Modular Knee System, curved tibial insert (CVD); polyethylene tibial insert, Sz 1, 10.0 mm; Ref 98-4031.
FDA device recall Z-1332-05 · posted 2005-08-12 · Terminated
Recall details
- Recalling firm
- Depuy Orthopaedics, Inc.
- Reason for recall
- An incomplete seal on the inner pouch allows exposure to oxygen, which may result in oxidation and would affect long-term performance of the implant.
- Root cause
- Other
- Status
- Terminated
- Product code
- JWH
- Quantity affected
- 5
- Distribution
- Nationwide, Argentina, Brazil, Canada, Caguas, Colombia, Ireland, Malaysia, Mexico, Panama, Peru, Singapore, South Africa, Sweden, Uruguay and Venezuela.
- Date initiated
- 2005-05-26
- Date posted
- 2005-08-12
- Date terminated
- 2005-12-02
- Location
- Warsaw, IN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| P.F.C.(TM) MODULAR KNEE SYSTEM (K884796) | Johnson & Johnson Professionals, Inc. | 1989-03-29 |