Z-1281-2022 Class II Ongoing
FDA device recall Z-1281-2022 was initiated by Beaver Visitec International, Inc. on Apr 26, 2022 and is designated Class II. 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 The recall status is ongoing. Affected quantity: 660 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 29, 2022
- Initiation Date
- Apr 26, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 660 units
Product Description
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
Distribution Pattern
US Nationwide distribution in the states of AZ, CA, CT, DC, FL, GA, IN, MA, MN, NV, SC, TX, WA.
Code Information
UDI-DI: 30886158010488 Lot Number: 6045693
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1281-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026