BD Integra 1ml Insulin Syringe with Retracting Precision Guide Needle 1 ml 29g 1/2'' (0.33mm x 13 mm) Re-Order No. 30528
FDA device recall Z-0582-2007 · posted 2007-03-03 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- The needle becomes detached from the hub/syringe
- Action taken
- Recall notification letters were sent via UPS second day air on January 27, 2007. Distributors were asked to provide end user contact information to recalling firm.
- Root cause
- Other
- Status
- Terminated
- Product code
- FMF
- Quantity affected
- 247,824 units
- Distribution
- Nationwide
- Date initiated
- 2007-01-27
- Date posted
- 2007-03-03
- Date terminated
- 2007-07-24
- Location
- Franklin Lakes, NJ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| BD INTEGRA SYRINGE (K023752) | Bd | 2003-02-07 |