BD 30G1/2" Precision Glide" Needle Needles are used for aspiration and injection of medications
FDA device recall Z-1009-2012 · posted 2012-02-13 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- Becton Dickinson has identified clogged needles.
- Action taken
- 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.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- FMI
- Quantity affected
- 480,000 units
- Distribution
- Nationwide Distribution including IL and NJ
- Date initiated
- 2011-10-08
- Date posted
- 2012-02-13
- Date terminated
- 2012-12-11
- Location
- Franklin Lakes, NJ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET (K021475) | Bd | 2002-07-19 |