BD 1 mL Allergist tray with 27 G x 1/2 in. BD Safety Glide.
FDA device recall Z-0404-06 · posted 2006-01-18 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- Safety mechanisms on the syringes are rotating too freely. This can result in the safety mechanism not holding its rotational position and increasing risk of an accidental needle-stick.
- Action taken
- Recall notifications were sent to all direct consignees and potential end users on 10/25/2005 via UPS second day air.
- Root cause
- Other
- Status
- Terminated
- Product code
- FMF
- Quantity affected
- 2495 cases -- 2495000 syringes
- Distribution
- Product was distributed nationwide to 450 consignees composed of wholesalers, hospitals, and medical supply distributors. There is a Canadian customer, Dufort & Lavigne, Montreal, Quebec, Canada. Gove
- Date initiated
- 2005-10-25
- Date posted
- 2006-01-18
- Date terminated
- 2006-06-21
- 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 |