Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)
FDA device recall Z-0530-05 · posted 2005-02-04 · Terminated
Recall details
- Recalling firm
- Interpore Cross International Inc
- Reason for recall
- Mislabeled.
- Action taken
- Firm sent recall letters on 1/18/2005 requesting return of product. A response form was enclosed.
- Root cause
- Other
- Status
- Terminated
- Product code
- MQP
- Quantity affected
- 63
- Distribution
- TN, MT, MI, CA, IN, PA, NJ, TX, KY, LA, CO.
- Date initiated
- 2005-01-14
- Date posted
- 2005-02-04
- Date terminated
- 2005-03-03
- Location
- Irvine, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MODIFICATION TO GEO STRUCTURE (K040168) | Interpore Cross Intl. | 2004-04-08 |