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 Kits
- Model numbers
- 1) Kit SKU DT22010B, UDI/DI 10653160351092, Lot number 25EBC888, 2) Kit SKU DT22790C, UDI/DI 10653160996965, Lot number 25EBO566, 3) Kit SKU DT22790C, Lot number 25EBD964 +10 more
- 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
Medline Kits are essential medical supplies used in various healthcare settings for procedures requiring sterilization and precision. They are often used in hospitals, clinics, and by healthcare providers to ensure patient safety and hygiene during medical interventions.
Why This Is Dangerous
The defect involves an open seal on the packaging of BD ChloraPrep Triple Swabsticks, which may compromise their sterility. This increases the risk of infection when used on patients.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers should stop using these kits to avoid potential health risks. The recall creates an immediate need for replacements, impacting healthcare providers and patients relying on these products.
Practical Guidance
How to identify if yours is affected
- Check the SKU and lot number on your medical kit packaging.
- Compare your product details with the recall announcement.
- If your product matches any listed SKU or lot number, it is affected.
Where to find product info
The SKU and lot numbers can usually be found on the outer packaging of the medical kits or on the accompanying documentation.
What timeline to expect
Expect a refund processing timeline of 4-6 weeks after returning the recalled product.
If the manufacturer is unresponsive
- Contact Medline Industries directly via phone or email.
- Document all communication attempts for your records.
- Consider reaching out to regulatory authorities if the company does not respond.
How to prevent similar issues
- Look for seals on packaging to ensure sterility when purchasing medical supplies.
- Check for FDA recalls before using medical products.
- Choose reputable brands known for quality assurance.
Documentation advice
Keep a copy of your purchase receipt and any correspondence with Medline regarding the recall.
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Product Details
The recall includes various Medline Kits with SKUs DT22010B, DT22790C, DYNDA2966A, DYNDC2208C, DYNDC3107, and others. The affected lots include 25EBC888, 25EBO566, 25EBD964, 25EBN178, and 25EBL624. These kits were distributed nationwide in the United States.
Key Facts
- Recall date: December 24, 2025
- Quantity recalled: 21,854 units
- Hazard classification: Class II
- Affected kits include multiple SKUs and lot numbers
- No injuries or deaths reported
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Safety Guide
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