Olympus DISPOSABLE GRASPING FORCEPS — Class II medical device recall Z-1122-2022
Terminated recall by Olympus Corporation of the Americas, reported 2022-06-01, distributed nationwide. Forceps do not comply with Olympus standards for the amount of force required to open and close the forceps
| Recall number | Z-1122-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2022-03-31 |
| Classified | 2022-05-20 |
| Reported by FDA | 2022-06-01 |
| Terminated | 2024-07-25 |
| Distributed | Nationwide (US) |
| Quantity | 1,386 units |
| Lot numbers | 01K, 02K, 03K, 04K, 05K, 06K, 07K, 08K, 09K, 0XK, 0YK, 0ZK, 11H, 11K, 12K, 13K, 14K, 15K, 16K, 17K, 18K, 19K, 1XK, 71K, 72K, 73K, 74K, 75K, 76K, 77H, 77K, 78K, 79K, 7XK, 7YK, 7ZK, 81K, 82K, 83K, 84K and 20 more |
Product
Olympus DISPOSABLE GRASPING FORCEPS, FG-51D
Reason for recall
Forceps do not comply with Olympus standards for the amount of force required to open and close the forceps
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-1122-2022. 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.