Microtek Medical, Inc. recalls Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN Patient Drape, 8mm…
Due to non-sterile products being labeled as sterile
Read the official notice →- Date
- 2025-06-18
- Country
- United States
- Brand
- Microtek Medical
- Product
- Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN Patient Drape, 8mm…
- Classification
- Class II
- Units
- U.S.: AL. AR, CA, CO, CT, FL, GA, IA, IL, IN, KY, MA, MI, NC, NY, OH, OR, TN,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Microtek Medical recalls
- 2024-08-28
USMicrotek Medical Inc. recalls 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).
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 · DeviceMicrotek Medical Inc.Distributed nationwide and internationally to Canada, Mexico, New Zealand,…Official notice →- 2023-08-09
- US
Microtek Medical Inc. recalls 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,…
Certain lots of the products have a Naphthalene odor.
FDA · DeviceMicrotek Medical Inc.Worldwide distribution - US Nationwide and the country of Canada.Official notice → - 2022-05-18
- US
Microtek Medical Inc. recalls TMJ Arthroscopy Drape, 85''x 96''
Latex content in product was labeled incorrectly as latex free.
Other drugs & medical recalls in the United States
- 2025-06-18
- US
Belmont Instrument LLC recalls Allon 2001. Part Number: 200-00263
An investigation into a report of the patient wrap (ThermoWrap), used with the Allon device, exceeding the set temperature determined that if: 1. The Human Sensor Board is disconnected from the Controller Board in the…
FDA · DeviceBelmont Instrument LLCWorldwide - US Nationwide distribution in the states of CA, DC, LA, MA, NM,…Official notice → - US
Mobius Mobility LLC recalls iBOT PMD with software version 01.05.24. Personal Mobility Device.
Software issue that could potentially lead to the device tipping over from Balance Mode.
FDA · DeviceMobius Mobility LLCUS Nationwide distribution in the states of CA, CO, FL, GA, IN, NC, NJ, OH,…Official notice → - US
Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, product code 40800BAXUS,
Baxter has identified a design issue which may cause the pump to detect the presence of a syringe flange when no syringe is loaded. When this issue occurs, the pumps 'user interface becomes stuck on the "Remove…
- US
Baxter Healthcare Corporation recalls 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles, Product Code 72600
The replacement rechargeable batteries inserted into the Welch Allyn PocketScope handles have the potential to cause a short circuit in the handle, which can lead to exposure to excessive heat and user burns.
- US
Microbiologics Inc recalls KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿ 17960; 0621K,…
Affected products were packaged with the incorrect KWIK STIK assembly resulting in the product containing the wrong microorganism. 0621K was packaged 01065K swabs; 01065K was packaged with 0621K swabs. This may lead to…
FDA · DeviceMicrobiologics IncUS Nationwide distribution in the states of California and Pennsylvania and…Official notice → - US
Contamac Solutions, Inc. recalls Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Contact lens insertion solution may lack sterility.
FDA · DeviceContamac Solutions, Inc.US Nationwide distribution in the states of AZ, CA, CO, FL, IL, IN, KS, KY,…Official notice →