Reported Jun 18, 2025 · Ongoing

Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN…

Microtek Medical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Microtek Medical, Inc. · 13000 Deerfield Pkwy Ste 300 · Alpharetta, GA · 30004-6118

Is this the product you have?

  • 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(01)10748426139429 These adapters function as accessories for a device or drape, serving to connect a drape's drain hose to a fluid management device. Their purpose is to reduce the opening of the drain hose to a smaller size
Lot codes and dates
  • Catalog NumberAP6MMN
  • UDI code(01)10748426139986
  • Lot/Batch Numbers
    • 5272JX0300
    • 7372JX3000
    • 4422JX1900
    • 1502JX0200
    • 5502JX0900
    • 1023JX0200
    • 6023JX0400
    • 1334JX1400
  • Catalog NumberAP8MMN
  • UDI code(01)10748426139429
  • Lot/Batch 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
Amount recalled
2,024 boxes

Where it was sold

Why it was recalled

Due to non-sterile products being labeled as sterile

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.