Device recall
Z-2119-2015: Hysto Pack, Non-sterile Part Number Description SA2059B MAJOR BASIN SA2220 HYSTO…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-2119-2015 |
|---|---|
| Recall event | 71113 |
| Product | Hysto Pack, Non-sterile Part Number Description SA2059B MAJOR BASIN SA2220 HYSTO PACK SA2220A HYSTO PACK |
| Product code | FSY |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 28, 2017 |
| FEI number | 1219930 |
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