BD 60 ml Syringe, Luer-Lok Tip Sterile; Cases : 160 (4 x 40) Shelf Carton: 40 BD; Franklin Lakes, NJ 07417 USA. Made in
FDA device recall Z-2374-2008 · posted 2008-09-18 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- Becton Dickinson identified the presence of open seals during an internal inspection process.
- Action taken
- Urgent: Product Recall letters were sent to Distributors and Syringe Customers on July 15, 2008 by UPS second day air. Customers are to immediately review their inventory, determine if they have any affected product, and remove the affected if they have any. Next customers should complete the enclosed Customer Packing List and BD will send a replacement product upon receipt of the returned product. Questions are to be directed to BD Customer Service at 1-888-237-2762, M-F, 8:00 AM to 5:00 PM EST.
- Root cause
- Package design/selection
- Status
- Terminated
- Product code
- FMF
- Quantity affected
- 1246 lots
- Distribution
- Nationwide Distribution.
- Date initiated
- 2008-07-15
- Date posted
- 2008-09-18
- Date terminated
- 2009-04-16
- Location
- Franklin Lakes, NJ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.