The Recall Desk

FDA (Devices) recall action 91488

Beaver Visitec International, Inc. recalled 2 products on 2023-03-08

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2023-03-08
Critical
0
Units
9,280

Why these products were recalled

Device packaging may contain open seals, compromising product sterility.

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–2 of 2

  • HighFDA (Devices)··2023-03-08

    CustomEyes kits recalled due to potential sterility compromise

    Beaver Visitec International is recalling 4640 units of CustomEyes kits because packaging may contain open seals that could compromise product sterility. Affected units were distributed to 26 U.S. states and internationally.

    Product
    CustomEyes kits
    Category
    Distribution
    27 states
  • HighFDA (Devices)··2023-03-08

    Ultracell Wick with Collection Bag Recalled for Compromised Packaging Sterility

    Beaver Visitec International recalls Ultracell Wick with 80cc Collection Bag due to packaging with potentially open seals that may compromise product sterility. The recall affects 4,640 units distributed across the United States and internationally.

    Product
    Ultracell Wick with 80cc Collection Bag, 20/box
    Category
    Distribution
    27 states