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Recall

Class II — Beaver Visitec International, Inc.

Recalling firmBeaver-Visitec International, Inc.
Registered facilityBeaver-Visitec International, Inc (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonOne lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
ProductConventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
Quantity1980 units
DistributionInternational distribution to the countries of Belgium, China, France, Germany, Greece, Italy, Jordan, Lithuania, Netherlands, Oman, Poland, Spain, Sweden.
Initiated2023-08-25
Classified2024-01-04
Recall numberZ-0632-2024
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Beaver Visitec International, Inc. (Z-0632-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93547/

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