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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 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.
Recall announced
January 7, 2026
Reported by FDA DEVICE
February 25, 2026
RecallRadar source check
March 4, 2026
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
- Locate the model number on the packaging or product label.
- Check if the model number matches any listed in the recall notice.
- 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.
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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
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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