Slit Knife 2 — Class II medical device recall Z-2740-2018
Terminated recall by Beaver Visitec, reported 2018-08-15, distributed in CA, IL, MD, MN, NJ, OH, PA. Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual packages within the correctly lab
| Recall number | Z-2740-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beaver Visitec, Waltham, MA, United States |
| Recall initiated | 2018-06-18 |
| Classified | 2018-08-09 |
| Reported by FDA | 2018-08-15 |
| Terminated | 2019-10-30 |
| Distributed | CA, IL, MD, MN, NJ, OH, PA |
| Countries outside the US | IL |
| Quantity | 440 |
| Reason classes | labeling |
| Lot numbers | 6001700 |
| Model numbers | 373726 |
Product
Slit Knife 2.6mm 45degree Bevel Up, Model Number 373726. for use in ophthalmic surgery.
Reason for recall
Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual packages within the correctly labeled shelf carton.
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-2740-2018. 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.