Wet-Field EraserRecalls & reported problems across all models
Beaver-Visitec International, Inc. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one Wet-Field Eraser model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 2
We found 2 models of Wet-Field Eraser by Beaver-Visitec International, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
2 FDA recall records name at least one of these models by its device identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Wet-Field Eraser recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- May 25, 2022Open, Classified
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Z-1594-2022 · Root cause: Environmental control · Recall details · FDA record ↗
- Apr 26, 2022Open, Classified
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
Z-1281-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Wet-Field Eraser models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Wet-Field® Eraser® 221251ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 recall0 reports
- Wet-Field® Eraser® 221265ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 recall0 reports
Other Beaver-Visitec International, Inc. products
All Beaver-Visitec International, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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