Device recall
Z-0593-2007: POOLE Suction Instrument, REF 0035040. MANUFACTURED FOR CONMED CORPORATION, 310…
FDA device recall · Class II · Conmed Corporation
Key facts
| Recall number (Z-number) | Z-0593-2007 |
|---|---|
| Recall event | 37346 |
| Product | POOLE Suction Instrument, REF 0035040. MANUFACTURED FOR CONMED CORPORATION, 310 Broad Street, Utica, NY 13501. ASSEMBLED IN MEXICO. |
| Product code | GCJ |
| Recalling firm | Conmed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 31, 2012 |
| FEI number | 3001451571 |
At a glance
- None Linked 510(k)s
- 10–99 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