Beaver Xstar Slit Knife 2 — Class II medical device recall Z-1111-2019
Terminated recall by Beaver Visitec, reported 2019-04-17, distributed nationwide. Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double Bevel knife however, the marking on
| Recall number | Z-1111-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beaver Visitec, Waltham, MA, United States |
| Recall initiated | 2019-03-12 |
| Classified | 2019-04-09 |
| Reported by FDA | 2019-04-17 |
| Terminated | 2020-08-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB, JP, NL |
| Reason classes | labeling |
| Lot numbers | 6008554 |
| Model numbers | 370824 |
Product
Beaver Xstar Slit Knife 2.4 mm, 45degree Double Bevel, Ophthalmic-utilized in Cataract and Glaucoma procedures REF # 370824 Product Usage: Ophthalmic techniques-utilized in Cataract and Glaucoma procedures
Reason for recall
Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double Bevel knife however, the marking on device shows a 2.75mm size 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-1111-2019. 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.