Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BEAVER-VISITEC INTERNATIONAL Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to Facility Temperature excursions (from June 2021-August 2021) prior...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mckesson Medical-Surgical Inc. Corporate Office directly.
Affected Products
BEAVER-VISITEC INTERNATIONAL, INC. Visitec CANNULA, LASIK IRR (10/BX)BVRVIS Catalog #585278
Quantity: 1 Box
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mckesson Medical-Surgical Inc. Corporate Office
Mckesson Medical-Surgical Inc. Corporate Office has 276 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report