Device recall
Z-1489-2008: Zimmer Hemovac Wound Drainage Device, Infection Control Kits, 400ml INF. CNTRL…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-1489-2008 |
|---|---|
| Recall event | 47233 |
| Product | Zimmer Hemovac Wound Drainage Device, Infection Control Kits, 400ml INF. CNTRL. Kit w/ 3/32" Drain, 2,4mm, 7Fr, PVC, 107cm, small, sterile, latex free, Rx only; Zimmer, Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio; REF 00-2550-001-10. |
| Product code | GCY |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 12, 2009 |
| FEI number | 1000220733 |
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