Device recall
Z-1610-2015: Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer…
FDA device recall · Class III · Zimmer Surgical Inc
Key facts
| Recall number (Z-number) | Z-1610-2015 |
|---|---|
| Recall event | 71057 |
| Product | Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer Surgical, Inc. Intended for post-operative collection of wound drainage. |
| Product code | GCY |
| Recalling firm | Zimmer Surgical Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 6, 2015 |
| FEI number | 1526350 |
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