BD 30 ml Syringe; Luer-Lok Tip Catalog # 309650 Becton Dickinson, Franklin Lakes, NJ.
FDA device recall Z-0586-2010 · posted 2009-12-29 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- Reports received of open seals on lot # 9175046, BD 30 ml Luer-Lok Syringes. This indicates product sterility may be compromised.
- Action taken
- Recall notification letters were sent to all distributors on 11/23/2009 by Federal Express. BD called all distributors to get customer lists and will start sending letter to customers commencing on December 8, 2009. Questions are directed to BD Customer Service at 1-888-237-2762, Monday Friday, 8:00 AM 5:00 PM Eastern Time.
- Root cause
- Other
- Status
- Terminated
- Product code
- FMF
- Quantity affected
- 166240 units
- Distribution
- Distributors nationwide.
- Date initiated
- 2009-11-23
- Date posted
- 2009-12-29
- Date terminated
- 2010-04-06
- Location
- Franklin Lakes, NJ
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