Device recall
Z-0088-2019: Unna-Z: Unna Boot Compression Wrap with Zinc Oxide and Calamine, Item Numbers…
FDA device recall · Class II · MEDLINE INDUSTRIES INC
Key facts
| Recall number (Z-number) | Z-0088-2019 |
|---|---|
| Recall event | 80972 |
| Product | Unna-Z: Unna Boot Compression Wrap with Zinc Oxide and Calamine, Item Numbers: a) NONUNNA3 and b) NONUNNA4 Product is packaged in a foil pouch, which is inserted in a box carton. There are 12 cartons in each case. |
| Product code | NEC |
| Recalling firm | MEDLINE INDUSTRIES INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 9, 2023 |
| FEI number | 1417592 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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