HIGHFDA DEVICE

Medline Surgical Drapes Recalled Over Sterility Issues

Medline Industries recalled 14.9 million surgical drapes on January 7, 2026. Calibration issues with sterilization equipment may impact sterility assurance levels. Patients and healthcare providers must stop using these products immediately.

Official notice
Medline Industries, LPHealth & Personal CareMedical Devices1) DYNJP2410UDI-DI: 10080196739691(each)40080196739692(case)

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
January 7, 2026
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
January 7, 2026
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
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, LP
Product type
Surgical Drapes
Model numbers
1) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case), Lot Number: 30525050127, 2) DYNJP2410, Lot Number: 30525070161, 3) DYNJP2410, Lot Number: 30525070250 +4 more
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 7, 2026

  2. Reported by FDA DEVICE

    February 25, 2026

  3. RecallRadar source check

    March 4, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

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 surgical drapes are used in medical settings to maintain a sterile environment during procedures. They are essential for preventing infections and ensuring patient safety.

Why This Is Dangerous

The calibration issues with sterilization equipment may result in non-sterile drapes reaching patients, increasing the risk of infections during surgeries.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Healthcare providers must urgently stop using the affected drapes, which disrupts operations and compromises patient safety.

Practical Guidance

How to identify if yours is affected

  1. Locate the model number on the packaging or product label.
  2. Check if the model number matches any listed in the recall notice.
  3. If unsure, contact Medline Industries for verification.

Where to find product info

Model numbers can be found on the product packaging or labels attached to the surgical drapes.

What timeline to expect

Expect 4-6 weeks for refund processing after the returned products are received.

If the manufacturer is unresponsive

  • Continue to follow up with Medline Industries via phone or email.
  • Document all communication attempts for your records.
  • Consider contacting the FDA if no response is received.

How to prevent similar issues

  • Ensure future purchases have clear certification of sterility.
  • Check for any recalls before purchasing medical supplies.
  • Consult with healthcare professionals regarding product safety.

Documentation advice

Keep copies of receipts, any correspondence with Medline, and photos of the product for your records.

Get instant alerts for Health & Personal Care recalls

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

No spamUnsubscribe anytime

Product Details

The recall affects various models of Medline surgical drapes, including DYNJP2410 and DYNJP2411. These products were distributed worldwide, with a total of 14,927,765 units recalled.

Key Facts

  • Recall date: January 7, 2026
  • Total units recalled: 14,927,765
  • Affected models include DYNJP2410, DYNJP2411
  • Health risk due to potential sterility issues

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
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
1) DYNJP2410
UDI-DI: 10080196739691(each)
40080196739692(case)
Lot Number: 30525050127
2) DYNJP2410
+7 more
Affected States
ALL
Report Date
February 25, 2026
Recall Status
ACTIVE

Related Recalls