Device recall
Z-0318-2022: The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN /…
FDA device recall · Class II · Magnolia Medical Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0318-2022 |
|---|---|
| Recall event | 88919 |
| Product | The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System - 21G, Wide Neck 2700-23-EN / Steripath Gen2 Blood Collection System - 23G, Wide Neck 27BD-21-EN / Steripath Gen2 Blood Collection System - 21G, Long Neck 27BD-23-EN / Steripath… |
| Product code | JKA |
| Recalling firm | Magnolia Medical Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2023 |
| 510(k) numbers | K192247 |
| FEI number | 3009976527 |
At a glance
- 1–9 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