Medical DeviceJun 18, 2025
Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI recall — FDA Z-1963-2025
Due to non-sterile products being labeled as sterile
Class IIFDA: OngoingMicrotek Medical, Inc.
Recall history in this database
Classification mix: Class II: 8.
Medical DeviceAug 28, 2024
Microtek Medical Bag Decanter II, REF 2002S recall — FDA Z-2640-2024
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Class IIFDA: OngoingMicrotek Medical Inc.
Medical DeviceAug 28, 2024
Microtek Medical Vial Decanter, REF 2006S recall — FDA Z-2642-2024
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Class IIFDA: OngoingMicrotek Medical Inc.
Medical DeviceAug 28, 2024
Microtek Medical Bottle Decanter, REF 2004S recall — FDA Z-2641-2024
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Class IIFDA: OngoingMicrotek Medical Inc.
Medical DeviceAug 28, 2024
Microtek Medical C-Flow Bag Decanter, REF 2000S recall — FDA Z-2639-2024
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Class IIFDA: OngoingMicrotek Medical Inc.
Medical DeviceAug 28, 2024
Microtek Medical Transfer Device, REF 2008S recall — FDA Z-2643-2024
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Class IIFDA: OngoingMicrotek Medical Inc.
Medical DeviceAug 9, 2023
Microtek Medical Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape recall — FDA Z-2250-2023
Certain lots of the products have a Naphthalene odor.
Class IIFDA: OngoingMicrotek Medical Inc.
Medical DeviceAug 9, 2023
Microtek Medical Equipment and table drapes and Surgical Room Turnover (SRT) Kits: (1) recall — FDA Z-2251-2023
Certain lots of the products have a Naphthalene odor.
Class IIFDA: OngoingMicrotek Medical Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Microtek Medical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.