--- title: "Microtek Medical Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Microtek Medical Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/microtek-medical-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Microtek Medical Inc. recall records **8** reported ongoing 9 records in this archive. Latest source date Apr 13, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Apr 13, 2025 FDA device enforcement ### [Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN Patient Drape, 8mm Adapter Plug Kit REF AP8MMN UDI code: ...](https://isitonrecall.com/recall/fda-device-z-1963-2025-microtek-patient-drape-ecolab-ap6mmn-patient-drape-6mm-adapter-plug-kit-ref-ap6mmn-udi-code-01-10748/) Due to non-sterile products being labeled as sterile Class II Reported ongoing Distribution: U.S.: AL. AR, CA, CO, CT, FL, GA, IA, IL, IN, KY, MA, MI, NC, NY, OH, OR, TN, TX, and VA O.U.S.: N/A [Official source for Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1963-2025%22) Jun 3, 2024 FDA device enforcement ### [C-Flow Bag Decanter, REF 2000S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).](https://isitonrecall.com/recall/fda-device-z-2639-2024-c-flow-bag-decanter-ref-2000s-packaged-on-a-form-fill-and-seal-machine-with-a-poly-tyvek-material-th/) 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 II Reported ongoing Distribution: Distributed nationwide and internationally to Canada, Mexico, New Zealand, Belize, and Hong Kong. [Official source for C-Flow Bag Decanter, REF 2000S. Packaged on a form, fill and seal machine with a poly/Tyvek mater...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2639-2024%22) Jun 3, 2024 FDA device enforcement ### [Bag Decanter II, REF 2002S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).](https://isitonrecall.com/recall/fda-device-z-2640-2024-bag-decanter-ii-ref-2002s-packaged-on-a-form-fill-and-seal-machine-with-a-poly-tyvek-material-then-p/) 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 II Reported ongoing Distribution: Distributed nationwide and internationally to Canada, Mexico, New Zealand, Belize, and Hong Kong. [Official source for Bag Decanter II, REF 2002S. Packaged on a form, fill and seal machine with a poly/Tyvek material ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2640-2024%22) Jun 3, 2024 FDA device enforcement ### [Bottle Decanter, REF 2004S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).](https://isitonrecall.com/recall/fda-device-z-2641-2024-bottle-decanter-ref-2004s-packaged-on-a-form-fill-and-seal-machine-with-a-poly-tyvek-material-then-p/) 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 II Reported ongoing Distribution: Distributed nationwide and internationally to Canada, Mexico, New Zealand, Belize, and Hong Kong. [Official source for Bottle Decanter, REF 2004S. Packaged on a form, fill and seal machine with a poly/Tyvek material ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2641-2024%22) Jun 3, 2024 FDA device enforcement ### [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).](https://isitonrecall.com/recall/fda-device-z-2642-2024-vial-decanter-ref-2006s-packaged-on-a-form-fill-and-seal-machine-with-a-poly-tyvek-material-then-pla/) 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 II Reported ongoing Distribution: Distributed nationwide and internationally to Canada, Mexico, New Zealand, Belize, and Hong Kong. [Official source for Vial Decanter, REF 2006S. Packaged on a form, fill and seal machine with a poly/Tyvek material th...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2642-2024%22) Jun 3, 2024 FDA device enforcement ### [Transfer Device, REF 2008S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).](https://isitonrecall.com/recall/fda-device-z-2643-2024-transfer-device-ref-2008s-packaged-on-a-form-fill-and-seal-machine-with-a-poly-tyvek-material-then-p/) 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 II Reported ongoing Distribution: Distributed nationwide and internationally to Canada, Mexico, New Zealand, Belize, and Hong Kong. [Official source for Transfer Device, REF 2008S. Packaged on a form, fill and seal machine with a poly/Tyvek material ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2643-2024%22) Jun 23, 2023 FDA device enforcement ### [Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape, 91 cm x 51 cm (36 in x 20 in), Model 63620RT, pkgd. 25/case, sterile; (2) Ecolab Microtek Banded Bag ...](https://isitonrecall.com/recall/fda-device-z-2250-2023-equipment-and-table-drapes-1-ecolab-banded-bag-with-rubberband-and-tape-91-cm-x-51-cm-36-in-x-20-in/) Certain lots of the products have a Naphthalene odor. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape, 91 cm x 51 cm (36 in ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2250-2023%22) Jun 23, 2023 FDA device enforcement ### [Equipment and table drapes and Surgical Room Turnover (SRT) Kits: (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile; (2)...](https://isitonrecall.com/recall/fda-device-z-2251-2023-equipment-and-table-drapes-and-surgical-room-turnover-srt-kits-1-ecolab-absorbent-table-cover-w-tran/) Certain lots of the products have a Naphthalene odor. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for Equipment and table drapes and Surgical Room Turnover (SRT) Kits: (1) Ecolab Absorbent Table Cove...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2251-2023%22) Apr 8, 2022 FDA device enforcement ### [TMJ Arthroscopy Drape, 85''x 96''](https://isitonrecall.com/recall/fda-device-z-1071-2022-tmj-arthroscopy-drape-85-x-96/) Latex content in product was labeled incorrectly as latex free. Class II Reported terminated Distribution: Distributed nationwide to CO, PA, and WI. [Official source for TMJ Arthroscopy Drape, 85''x 96''](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1071-2022%22) ## Reasons in these listed records - Due to non-sterile products being labeled as sterile - During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film. - Certain lots of the products have a Naphthalene odor. - Latex content in product was labeled incorrectly as latex free. These examples come from this result page and are not a ranking of every recall reason. ## Checking Microtek Medical Inc. ### Is there a recall on microtek medical inc. right now? This archive contains 9 records, including 8 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Microtek Medical Inc.](https://isitonrecall.com/check/?q=Microtek%20Medical%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)