Beaver Visitec recalls 18GA Blunt Tip Wet-Field Erasers with incorrect product shipped. Affected units have a bevel tip instead of blunt tip. No action needed as the product is safe for use.
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
Beaver Visitec recalls certain Wet-Field Erasers that were shipped with the wrong tip type. The recalled items have a bevel tip instead of the intended blunt tip. This does not pose a safety risk and no action is required.
The recalled items have a bevel tip instead of the intended blunt tip. This difference in tip design does not affect the product's safety or functionality for medical use. The hazard is purely a labeling error and not a safety issue.
Medical professionals who use the Wet-Field Eraser for tissue removal and bleeding control may have received the incorrect product. The risk is minimal as the product is safe for use.
Check for the product name 'Wet-Field Eraser', 18GA Blunt Tip, 45Deg. with part number 221251 or UDI-DI 30886158010488. The incorrect product has a bevel tip instead of blunt tip.
Verify the tip type on the product: the recalled items have a bevel tip instead of the intended blunt tip.
No, the product is safe for use. The recall is due to a labeling error, not a safety hazard.
No action is needed as the product is safe for use. The recall is for incorrect product labeling, not a safety issue.
Check for part number 221251 or UDI-DI 30886158010488 on the product label.
We’ve drafted a message you can send Beaver Visite: 18GA Blunt Tip to request your refund or repair — edit it as you like.
Subject: Recall Z-1281-2022 — Beaver Visite: 18GA Blunt Tip Beaver Visite: 18GA Blunt Tip Hello, I own a Beaver Visite: 18GA Blunt Tip that is covered by recall Z-1281-2022 from Beaver Visite: 18GA Blunt Tip. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
