Device recall
Z-0881-2008: PERFEKTUM TOOMEY EVACUATING SYRINGES, REF/Part # 5047, DESCRIPTION: 30CC LOCK…
FDA device recall · Class III · Popper & Sons Inc
Key facts
| Recall number (Z-number) | Z-0881-2008 |
|---|---|
| Recall event | 46322 |
| Product | PERFEKTUM TOOMEY EVACUATING SYRINGES, REF/Part # 5047, DESCRIPTION: 30CC LOCK TIP, RX ONLY, NON-STERILE. Manufactured By: Popper & Sons, Inc. New Hyde Park, NY. 11040. |
| Product code | FMI |
| Recalling firm | Popper & Sons Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 12, 2008 |
| FEI number | 2414164 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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