BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950.
FDA device recall Z-1525-06 · posted 2006-09-28 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- BD received reports of needle assembly disengagement from the syringe.
- Action taken
- Recall letters were sent to all wholesalers and end users on 7/28/2006.
- Root cause
- Other
- Status
- Terminated
- Product code
- MEG
- Quantity affected
- 1,294,200 units
- Distribution
- Nationwide.
- Date initiated
- 2006-07-24
- Date posted
- 2006-09-28
- Date terminated
- 2007-12-03
- 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 |
|---|---|---|
| BECTON DICKINSON SYRINGE (K992734) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1999-10-01 |