BD 60ml Syringe Luer-Lok tip, Sterile, BD, Franklin Lakes, NJ 07417, Made in USA.
FDA device recall Z-1811-2009 · posted 2009-08-12 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- Insufficient Seal: Becton Dickinson received complaints of insufficient/open seals on one lot of 60 ml Luer-Lok Syringes.
- Action taken
- Becton Dickinson issued an "Urgent: Product Recall" notice via UPS tracking dated July 7, 2009 to all distributors informing them of the affected product. The firm asked all distributors to identify end customers in an attempt to notify all customers. The firms asks that all affected product be returned. Further questions should be directed to BD Customer Service representatives at 1-888-237-2762.
- Root cause
- Packaging process control
- Status
- Terminated
- Product code
- FMF
- Quantity affected
- 133,600 units
- Distribution
- Nationwide Distribution -- Including states of IL, CA, VA, PA, and FL.
- Date initiated
- 2009-07-07
- Date posted
- 2009-08-12
- Date terminated
- 2009-10-02
- Location
- Franklin Lakes, NJ
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