Device recall
Z-2518-2021: Omnisound Gel, 250 ml bottle and 5 L container; and EcoGel 200, 250 ml bottle…
FDA device recall · Class I · Accelerated Care Plus Corporation
Key facts
| Recall number (Z-number) | Z-2518-2021 |
|---|---|
| Recall event | 88602 |
| Product | Omnisound Gel, 250 ml bottle and 5 L container; and EcoGel 200, 250 ml bottle; Manufactured by Eco-Med. For use in ultrasound procedures. |
| Product code | ITX |
| Recalling firm | Accelerated Care Plus Corporation |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K955246 |
| FEI number | 1000119345 |
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