Recalls / —
—#47690
Product
BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950.
- FDA product code
- MEG — Syringe, Antistick
- Device class
- Class 2
- Medical specialty
- General Hospital
- 510(k) numbers
- K992734
- Affected lot / code info
- Reorder Number: 305945 Lot: 5312395 and 5312394. Reorder Number: 305950 Lot: 5319508 and 5300175.
Why it was recalled
BD received reports of needle assembly disengagement from the syringe.
Root cause (FDA determination)
Other
Action the firm took
Recall letters were sent to all wholesalers and end users on 7/28/2006.
Recalling firm
- Firm
- Becton Dickinson & Company
- Address
- 1 Becton Dr, Franklin Lakes, New Jersey 07417-1815
Distribution
- Distribution pattern
- Nationwide.
Timeline
- Recall initiated
- 2006-07-24
- Posted by FDA
- 2006-09-28
- Terminated
- 2007-12-03
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #47690. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.