Device recall
Z-2229-2021: Grasper/Retriever, Alligator Jaw 2.4 mm x 5 mm x 230 cm Catalog Number: 7208…
FDA device recall · Class II · Shent USA, Inc.
Key facts
| Recall number (Z-number) | Z-2229-2021 |
|---|---|
| Recall event | 88136 |
| Product | Grasper/Retriever, Alligator Jaw 2.4 mm x 5 mm x 230 cm Catalog Number: 7208 Intended use: single use accessory devices used through the working channel of a GI endoscope |
| Product code | OCZ |
| Recalling firm | Shent USA, Inc. |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K974300 |
| FEI number | 1222168 |
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