FDA Recall
Terminated
BD 30G1/2" Precision Glide" Needle Needles are used for aspiration and injection of medications
Recall: Z-1009-2012
·
Initiated October 8, 2011
Recall
- Recall Number
- Z-1009-2012
- Event Number
- 60988
- Firm
- Becton Dickinson & Company
- FEI Number
- 2243072
- Product Code
- FMI
- Status
- Terminated
- Root Cause
- Device Design
- Initiated
- October 8, 2011
- Posted
- February 13, 2012
- Terminated
- December 11, 2012
- Address
- 1 Becton Dr, Franklin Lakes, NJ, 07417-1815
Description
BD 30G1/2" Precision Glide" Needle Needles are used for aspiration and injection of medications
Reason
Becton Dickinson has identified clogged needles.
Action
Becton Dickinson sent Urgent Product Recall letters dated October 18, 2011 and October 17, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to check their inventory to deterine if they have any of the affected product. If they have affected product customers should return the product to Beckton Dickinson. For any questions regarding this recall call 201-847-4344.
Distribution
Nationwide Distribution including IL and NJ
Quantity
480,000 units