BD 20 ml Syringe Luer-Lok Tip Sterile, Do not reuse; Catalog Number 309661.
FDA device recall Z-1488-2009 · posted 2009-06-24 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- Potential for compromised sterility: Insufficient packaging seals.
- Action taken
- Becton Dickinson sent Urgent Product Recall letters on April 30, 2009 to all direct customers. Questions are to be directed to BD Customer Service at 1-888-237-2762. Letters to customers of distributors went out on May 12, 2009.
- Root cause
- Nonconforming Material/Component
- Status
- Terminated
- Product code
- FMF
- Quantity affected
- 201,600 units
- Distribution
- Nationwide Distribution.
- Date initiated
- 2009-04-30
- Date posted
- 2009-06-24
- Date terminated
- 2009-09-28
- Location
- Franklin Lakes, NJ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.