Device recall
Z-0650-2022: Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
FDA device recall · Class II · Merete Medical GmbH
Key facts
| Recall number (Z-number) | Z-0650-2022 |
|---|---|
| Recall event | 89482 |
| Product | Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only |
| Product code | JDR |
| Recalling firm | Merete Medical GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 16, 2023 |
| 510(k) numbers | K151762 |
| FEI number | 3002949614 |
At a glance
- 1–9 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