HIGH

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.

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

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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

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.

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

  • 104,004 units recalled
  • 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

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

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

Related Recalls

Health & Personal Care
HIGH

Medline recalls 14,379 Olympus biopsy valve kits over rubber fragments in 2026 recall

Medline Industries is recalling 14,379 bronchoscopy kits containing Olympus biopsy valves distributed nationwide in the United States. Olympus reports rubber fragments detaching from the valve slit, which could leave a foreign body in a patient’s tracheobronchial tree and may require removal. Hospitals should stop using the affected kits immediately and follow Medline’s recall instructions.

Medline Industries
Kits contain
Read more
Health & Personal Care
HIGH

Medline ENFIT G-Tube Connector ENFIT1010GC Recalled for Leakage Risk (651,789 Units, 2026)

Medline Industries recalled 651,789 ENFIT G-TUBE connectors (ENFIT1010GC) sold worldwide, including the United States and Canada. The connectors were not manufactured to required dimensional specifications and may not seal properly with ENFit-style devices, which could lead to leakage. Healthcare facilities and patients should stop using this device immediately and follow recall instructions from

Medline Industries
Connectors were
Read more
Health & Personal Care
HIGH

Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)

Medline Industries recalled 88 units of the Sterile Extremity Pack DYNJ45701B after finding that kits labeled as sterile had not undergone sterilization. The affected distribution covered Florida, Maryland, New Jersey and Tennessee. Hospitals and clinics should stop using the kit immediately and follow Medline's recall instructions.

Medline Industries
Convenience kits
Read more
Health & Personal Care
HIGH

Medline Industries Recalls 22 Sterile Convenience Kits DYNJ0382730O, DYNJ61038B (2025)

Medline Industries, LP recalled 22 sterile convenience kits distributed to Florida, Maryland, New Jersey and Tennessee after determining the kits labeled as sterile had not undergone sterilization. The sterility lapse creates an infection risk for patients. Healthcare facilities and patients should stop using the kits and follow the recall instructions from Medline and the FDA.

Medline Industries
Convenience kits
Read more