RegWardenFDA facility compliance records
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
ReasonPack and pouch label is missing the manufacturing and expiration date.
ProductBVI Visitec Irrigation Handle (20/SP)- Intended to be fit with a cannula for irrigation of the eye Catalog Number: 581012
Quantity3,000 units (US and OUS)
DistributionWorldwide distribution - US Nationwide and the countries of AUSTRALIA, CANADA, GERMANY, SWITZERLAND, UNITED KINGDOM.
Initiated2024-02-02
Classified2024-03-14
Recall numberZ-1294-2024
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-1294-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93951/

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