TC-PLUS Tibial Insert 2; 15mm, Model 25309
FDA device recall Z-0014-06 · posted 2005-10-07 · Terminated
Recall details
- Recalling firm
- Plus Orthopedics USA
- Reason for recall
- Did not meet specifications.
- Action taken
- Recall was by scripted telephone conversations to two consignees. Products were returned under RMA.
- Root cause
- Other
- Status
- Terminated
- Product code
- JWH
- Quantity affected
- 21
- Distribution
- Arizona, California, Idaho, New York, Texas, and Virginia
- Date initiated
- 2005-08-03
- Date posted
- 2005-10-07
- Date terminated
- 2006-06-16
- Location
- San Diego, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| TC-PLUS SOLUTION KNEE (K000666) | Plus Orthopedics | 2000-10-13 |