Device recall
Z-0619-2009: BD 1 ml Integra TB Syringe with Retracting Precision Glide Needle; 1 ml 27 g 1/2…
FDA device recall · Class III · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-0619-2009 |
|---|---|
| Recall event | 50235 |
| Product | BD 1 ml Integra TB Syringe with Retracting Precision Glide Needle; 1 ml 27 g 1/2 (0.4mm x 13 mm); Sterile; REF # 305298 BD, Franklin Lakes, NJ 07417. Made in USA Syringes for use in aspiration and injection of medications. |
| Product code | MEG |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 27, 2009 |
| 510(k) numbers | K023752 |
| FEI number | 2243072 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database