Conventional Knife Crescent 2 — Class II medical device recall Z-0632-2024
Ongoing recall by Beaver Visitec International, Inc., reported 2024-01-10. One lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
| Recall number | Z-0632-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beaver Visitec International, Inc., Waltham, MA, United States |
| Recall initiated | 2023-08-25 |
| Classified | 2024-01-04 |
| Reported by FDA | 2024-01-10 |
| Countries outside the US | BE, CN, DE, ES, FR, GR, IT, JO, LT, NL, OM, PL, SE |
| Quantity | 1,980 units |
| UPC / GTIN / UDI-DI | 30886158000571 |
| Lot numbers | 6054027 |
| Model numbers | 373807 |
Product
Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
Reason for recall
One lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
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-0632-2024. 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.