Xstar Safety Slit Knife — Class II medical device recall Z-2162-2024
Ongoing recall by Beaver Visitec International, Inc., reported 2024-06-26, distributed nationwide. The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being
| Recall number | Z-2162-2024 |
|---|---|
| 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 | 2024-05-10 |
| Classified | 2024-06-20 |
| Reported by FDA | 2024-06-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, GB, IT |
| Quantity | 126 units |
| UPC / GTIN / UDI-DI | 00886158001652 |
| Lot numbers | 6058854, 6068025, 6068285, 6068524 |
| Model numbers | 378227 |
Product
Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227, a component of CustomEye Kits, Numbers 584562, 5800109
Reason for recall
The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down).
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-2162-2024. 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.