PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION — Class II medical device recall Z-1481-2022
Completed recall by Aesculap Implant Systems LLC, reported 2022-08-10, distributed nationwide. Endoscopic graspers may become separated at the weld from handle to the shaft of the device.
| Recall number | Z-1481-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap Implant Systems LLC, Center Valley, PA, United States |
| Recall initiated | 2020-04-01 |
| Classified | 2022-07-29 |
| Reported by FDA | 2022-08-10 |
| Distributed | Nationwide (US) |
| Quantity | 3,392 |
| UPC / GTIN / UDI-DI | 04046955083374 |
| Lot numbers | M45041, M45399, M45711, M46069, M46350, M47462, M47893, M48115, M48279, M48346, M48467, M48596, M48753, M48848, M48907, M49375, M49435, M49632, M49683, M49711, M49867, M55796 |
Product
PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
Reason for recall
Endoscopic graspers may become separated at the weld from handle to the shaft of the device.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1481-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.