BD 30ml Syringe Luer-Lok tip Sterile BD, Franklin Lakes, NJ Made in USA
FDA device recall Z-0719-2007 · posted 2007-04-05 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- The unit label on a limited number of syringes is incorrect, citing a 20 ml size. All other levels of labeling are correct, identifying the product as 30 ml size.
- Action taken
- Distributors were sent recall notification letters on February 1, 2007 Recall notification letters were sent to all direct accounts and potential end users via UPS second day air on February 15, 2007.
- Root cause
- Other
- Status
- Terminated
- Product code
- FMF
- Quantity affected
- 332,400 units
- Distribution
- Nationwide.
- Date initiated
- 2007-02-15
- Date posted
- 2007-04-05
- Date terminated
- 2007-07-19
- 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 |
|---|---|---|
| BECTON DICKINSON SYRINGE (K980987) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1998-06-11 |