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Microtek Medical Inc. recalls Vial Decanter, REF 2006S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products t
Recalled August 28, 2024 · FDA recall Z-2642-2024 · Microtek Medical
Hazard
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film. · FDA Class II
Units
30,435 cases (1,521,750 units)
Sold at
Distributed nationwide and internationally to Canada, Mexico, New Zealand, Belize, and Hong Kong.
Description
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Product
Vial Decanter, REF 2006S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).
Manufacturer(s)
Microtek Medical Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →