BVI Wet -Field Eraser — Class II medical device recall Z-1281-2022
Ongoing recall by Beaver Visitec International, Inc., reported 2022-06-29, distributed nationwide. Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped containing incorrect product a Wet-Fie
| Recall number | Z-1281-2022 |
|---|---|
| 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 | 2022-04-26 |
| Classified | 2022-06-22 |
| Reported by FDA | 2022-06-29 |
| Distributed | Nationwide (US) |
| Quantity | 660 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 30886158010488 |
| Lot numbers | 6045693 |
| Model numbers | 221251 |
Product
BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency electrical current Part Number: 221251
Reason for recall
Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped containing incorrect product a Wet-Field Eraser, 18GA Bevel Tip, Straight, Part Number: 221250
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-1281-2022. 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.