Wet-Field Hemostatic Eraser Bipolar 25G — Class II medical device recall Z-1801-2018
Terminated recall by Beaver-Visitec International Inc., reported 2018-05-16, distributed nationwide. Products were packaged with incorrect labeling,
| Recall number | Z-1801-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beaver-Visitec International Inc., Waltham, MA, United States |
| Recall initiated | 2018-02-26 |
| Classified | 2018-05-10 |
| Reported by FDA | 2018-05-16 |
| Terminated | 2019-10-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 1,025 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 30886158010549 |
| Lot numbers | 6001035 |
| Model numbers | 221267 |
Product
Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
Reason for recall
Products were packaged with incorrect labeling,
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-1801-2018. 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.