Device recall
Z-2720-2016: ReliaMed Alginate/CMC. Each dressing is packed in a pouch (primary packaging)…
FDA device recall · Class II · Advanced Medical Solutions Ltd.
Key facts
| Recall number (Z-number) | Z-2720-2016 |
|---|---|
| Recall event | 75033 |
| Product | ReliaMed Alginate/CMC. Each dressing is packed in a pouch (primary packaging), each pouch is packed in a carton (secondary packaging) holding multiple (depending on stock keeping unit) pouches and each carton contains one (1) Instructions For Use (IFU) leaflet. |
| Product code | FRO |
| Recalling firm | Advanced Medical Solutions Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 23, 2016 |
| FEI number | 3003080333 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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