Device recall
Z-2066-2019: Medline Primary Warmer Pack, Product No. DYNJ52510A. The Medline Primary Warmer…
FDA device recall · Class I · Medline Industries Inc
Key facts
| Recall number (Z-number) | Z-2066-2019 |
|---|---|
| Recall event | 82940 |
| Product | Medline Primary Warmer Pack, Product No. DYNJ52510A. The Medline Primary Warmer Pack contains the recalled Vyaire enFlow Disposable Cartridge, which is the subject of this recall, and the recalled BD Alaris Pump Infusion Set (RES#82951) Product Usage: The Vyaire enFlow Disposable Cartridges contain… |
| Recalling firm | Medline Industries Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 1, 2021 |
| FEI number | 1417592 |
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