Device recall
Z-2393-2021: Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This…
FDA device recall · Class II · Magnolia Medical Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-2393-2021 |
|---|---|
| Recall event | 88338 |
| Product | Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer Blood Collection or Urine Collection Tubes. |
| Product code | JKA |
| Recalling firm | Magnolia Medical Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 22, 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