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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Microtek and Ecolab Patient Drapes Recalled for Incorrect Sterile Labeling

Agency Publication Date: June 12, 2025
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Summary

Microtek Medical, Inc. is recalling approximately 2,024 boxes of Microtek and Ecolab Patient Drapes and Adapter Plug Kits. These kits, used to connect drainage hoses to medical fluid devices, are being recalled because products that are not sterile were incorrectly labeled and sold as sterile. No injuries or infections have been reported to date, but these items were distributed to hospitals and clinics across 20 states.

Risk

Using medical equipment that is falsely labeled as sterile creates a significant risk of bacterial contamination and serious infection during medical procedures. Patients could be exposed to pathogens in environments where sterility is required for safety.

What You Should Do

  1. The recalled products are Microtek and Ecolab Patient Drape kits, specifically the 6mm Adapter Plug Kit (model AP6MMN) and the 8mm Adapter Plug Kit (model AP8MMN).
  2. To identify if you have an affected product, check the label for catalog numbers AP6MMN (UDI 10748426139986) or AP8MMN (UDI 10748426139429).
  3. Check the lot or batch number printed on the packaging. See the Affected Products section below for the full list of affected codes.
  4. Stop using the recalled product immediately to prevent patient infection.
  5. Contact the manufacturer or your distributor to arrange for the return, replacement, or correction of the recalled units.
  6. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Microtek Patient Drape ECOLAB (6mm Adapter Plug Kit)
Variants: 6mm Adapter Plug
Model / REF:
AP6MMN
Lot Numbers:
5272JX0300
7372JX3000
4422JX1900
1502JX0200
5502JX0900
1023JX0200
6023JX0400
1334JX1400
UDI:
10748426139986

These adapters connect a drape's drain hose to a fluid management device.

Product: Microtek Patient Drape ECOLAB (8mm Adapter Plug Kit)
Variants: 8mm Adapter Plug
Model / REF:
AP8MMN
Lot Numbers:
3454LR3700
2484LR8000
1494LR0600
4025LR2800
2035LR5000
5342JX0600
3292JX0500
4372JX1700
5422JX0600
1402JX1500
4422JX1800
5502JX1000
1023JX3400
5133JX0100
3143JX1100
1173JX1800
6143JX0300
5213JX4000
4233JX1400
5243JX3700
6253JX1400
4293JX2400
1343JX1000
4353JX7800
2373JX0600
5443JX2500
3453JX2900
4463JX1200
3493JX1400
6503JX0300
2034JX1100
1044JX3400
5074JX1500
1104JX1100
5164JX0500
5164JX0700
5164JX0600
5184JX0800
5224JX1400
5234JX3400
1254JX0300
4304JX1100
2334JX1800
UDI:
10748426139429

These adapters connect a drape's drain hose to a fluid management device.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96747
Status: Active
Manufacturer: Microtek Medical, Inc.
Sold By: Microtek Medical, Inc.; Ecolab
Manufactured In: United States
Units Affected: 2,024 boxes
Distributed To: Alabama, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Massachusetts, Michigan, North Carolina, New York, Ohio, Oregon, Tennessee, Texas, Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.