HIGHFDA DEVICE

Medline Medcrest Surgical Gowns Recalled 104,004 Units for Delamination Risk (2026)

Medline recall covers 104,004 Medcrest Surgical Gowns sold nationwide and internationally due to premature fabric delamination risk. Delamination can delay patient care in surgery and raise infection risk. Stop using the affected gowns and follow the manufacturer’s recall instructions immediately.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
January 28, 2026
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medline Industries
Product type
Surgical Gowns
Model numbers
MDTGXC4J5XL, MDTGXC4JL, MDTGXC4JXL, MDTGXC4JXXL, MDTGXP4JL, MDTGXP4JXL, MDTGXP4JXXL, MDTL1002862EF +1 more
Colors
GREEN
Sizes
L, XL, XXL
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 28, 2026

  2. Reported by FDA DEVICE

    March 18, 2026

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

Medline Medcrest Surgical Gowns are disposable gowns used in surgical settings. They are distributed nationwide in the US and internationally.

Why This Is Dangerous

Fabric delamination can occur with laundering, potentially delaying surgery and increasing infection risk if used.

Industry Context

This recall is not identified as part of a broader industry pattern in the provided data.

Real-World Impact

Hospitals may need to identify and replace affected gowns to prevent delays and infection risk during procedures.

Practical Guidance

How to identify if yours is affected

  1. Identify gowns by model numbers MDTGXC4J5XL, MDTGXC4JL, MDTGXC4JXL, MDTGXC4JXXL, MDTGXP4JL, MDTGXP4JXL, MDTGXP4JXXL, MDTL1002862EF, MDTZ1000893AJ.
  2. Check for labeling with GREEN color and panel/draping indicators as shown in the recall.
  3. Refer to UDI-DI numbers listed in the recall documentation for exact matching.

Where to find product info

Look on the packaging, labeling, and cuff tags for model numbers and UDI-DI identifiers.

What timeline to expect

Recall remedies are issued by the manufacturer; processing times vary and may take weeks.

If the manufacturer is unresponsive

  • Document all communications with suppliers
  • Escalate to hospital risk management or FDA recall contacts if needed.

How to prevent similar issues

  • Inspect laundering instructions on gown packaging before laundering.
  • Prefer gowns with clearer or standardized laundering guidelines.
  • Maintain a current recall log and verify shipments against recall lists.

Documentation advice

Keep a copy of the recall notice, take photos of labels and tags, and document all correspondence with the supplier.

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Product Details

Model numbers listed in recall: MDTGXC4J5XL, MDTGXC4JL, MDTGXC4JXL, MDTGXC4JXXL, MDTGXP4JL, MDTGXP4JXL, MDTGXP4JXXL, MDTL1002862EF, MDTZ1000893AJ. Distribution: Domestic distribution nationwide in the United States; international distribution to Panama, United Arab Emirates, Virgin Islands, Saudi Arabia, India, Chile, and Canada. Quantity: 104,004 units. Sold at: Unknown. Price: Unknown.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 9 listed model numbers
  • Domestic US nationwide distribution; international distribution to 7 countries
  • High-hazard class II recall
  • UDI-DI style identifiers included in model list

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

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

Product Details

Model Numbers
MDTGXC4J5XL
MDTGXC4JL
MDTGXC4JXL
MDTGXC4JXXL
MDTGXP4JL
+4 more
Affected States
ALL
Report Date
March 18, 2026
Recall Status
ACTIVE

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