BD 5 ml Syringe Luer Lok Tip Bulk Sterile Convenience Pak. Latex Free . Sterile. Reorder Number: 309703, BD, Franklin La
FDA device recall Z-0914-2008 · posted 2008-04-16 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- Defective Seal: The convenience trays may have open seals, which can adversely impact tray sterility.
- Action taken
- BD notified distributors by an Urgent Product Recall Letter sent via UPS on January 7, 2008. In addition, the firm sent an Urgent Product Recall Letter on January 11, 2008 to customers identified by the distributors. The letter instructed the users to remove the product from its inventory and to return affected products to the firm using an enclosed customer packing list. For additional information, contact 1-888-237-2762.
- Root cause
- Packaging
- Status
- Terminated
- Product code
- FMF
- Quantity affected
- 1,754,100
- Distribution
- Nationwide, including the states of CA, NY, MO, MA, IL, OH, TN, TX, MI, LA, MO, ID, GA, NE, SC and FL.
- Date initiated
- 2008-01-07
- Date posted
- 2008-04-16
- Date terminated
- 2008-05-19
- Location
- Franklin Lakes, NJ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.