Quick Facts at a Glance
- Recall Date
- December 24, 2025
- 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
- Medical Convenience Kits
- Model numbers
- UDI/DI 10195327379292, Lot Number 25EBJ785
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 24, 2025
Reported by FDA DEVICE
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
About This Product
The Medline Sterile Resection Pack is commonly used in medical procedures to maintain sterility and prevent infections. Healthcare providers rely on these kits for their essential components during patient care.
Why This Is Dangerous
The open seal on the BD ChloraPrep Triple Swabsticks can lead to contamination, posing a risk of infection during medical procedures.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients and healthcare providers must stop using the affected kits to avoid the risk of infection, which can lead to serious health complications.
Practical Guidance
How to identify if yours is affected
- Check the SKU DYNDL1980A on the packaging.
- Verify the lot number 25EBJ785 if applicable.
- Confirm the product is from the recall notice.
Where to find product info
The SKU and lot number can typically be found on the product packaging or label.
What timeline to expect
Expect a response regarding refunds or replacements within 4-6 weeks of contacting Medline.
If the manufacturer is unresponsive
- Document all correspondence with Medline.
- Follow up via phone or email.
- Consider filing a complaint with the FDA if issues persist.
How to prevent similar issues
- Always inspect medical kits for damaged or open seals before use.
- Purchase from reputable suppliers to ensure product integrity.
- Verify that products have up-to-date certifications and are not expired.
Documentation advice
Keep records of your purchase, photos of the product, and any communication with Medline for future reference.
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Product Details
The recalled product is the Sterile Resection Pack, SKU DYNDL1980A. It includes BD ChloraPrep Triple Swabsticks. The kits were distributed in the United States.
Key Facts
- Open seal may compromise sterility
- No reported injuries or incidents
- Contact Medline for further instructions
- Nationwide distribution in the US
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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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