HIGH

23,568 Medline Surgical Drapes Recalled Over Infection Risk

Medline Industries recalled 23,568 surgical drapes on January 28, 2026, after reports of fabric delamination during laundering. The delamination may delay patient care and increase the risk of infection. Health care providers and facilities must stop using these drapes immediately and follow the manufacturer's instructions for a remedy.

Quick Facts at a Glance

Recall Date
January 28, 2026
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter

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About This Product

Medline Surgical Drapes are designed for use in medical procedures, providing a sterile barrier during surgeries. Healthcare providers widely use these drapes to maintain cleanliness and reduce infection risks during patient care.

Why This Is Dangerous

The risk arises when the fabric of the surgical drapes delaminates, leading to compromised sterility. This can result in infection if the drapes fail to provide the necessary protection during procedures.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall affects patient care timelines, as surgeries may be delayed due to the need for alternative drapes. The risk of infection can elevate concerns among healthcare professionals regarding safety and outcomes.

Practical Guidance

How to identify if yours is affected

  1. Check the model number and UDI code to see if they match the recalled surgical drapes.
  2. Inspect for visual signs of delamination if possible.
  3. Consult the manufacturer’s website for updates and detailed recall information.

Where to find product info

The model numbers and UDI codes are located on the packaging or labels of the surgical drapes.

What timeline to expect

Expect processing for refunds or replacements to take approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Reach out to Medline Industries, LP directly for further assistance.
  • Document all interactions you have regarding the recall.

How to prevent similar issues

  • Look for surgical drapes with updated laundering instructions.
  • Purchase drapes that meet current medical standards.
  • Verify the safety history of products with healthcare providers.

Documentation advice

Keep records of your purchase, any communications with the manufacturer, and photographs of the products as evidence.

Product Details

Models affected include MDTBTCS6070GN, MDTBTCS6090GN, MDTDXUNDBGN, MDTMAYOXGN, and MDTZ1003656GN. Sold widely in the U.S. and internationally to countries including Panama, UAE, Virgin Islands, Saudi Arabia, India, Chile, and Canada.

Reported Incidents

No incidents or injuries have been reported.

Key Facts

  • Quantity recalled: 23,568 units
  • Recall initiated on: January 28, 2026
  • Distribution: Domestic and international
  • Classification: Class II
  • Risk of infection if delaminated drapes are used
View Original Recall on FDA - Medical Devices

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Safety Guide

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeSurgical Drapes
Sold At
Multiple Retailers

Product Details

Model Numbers
MDTBTCS6070GN
MDTBTCS6090GN
MDTDXUNDBGN
MDTMAYOXGN
MDTZ1003656GN
Affected States
ALL
Report Date
March 18, 2026
Recall Status
ACTIVE

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