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 10653160990666, Lot Number 25EBC648
- 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 medical convenience kits are used in medical settings for procedures requiring sterilized applicators. These kits are typically utilized in circumcision and other minor surgical procedures.
Why This Is Dangerous
The open seal on the packaging of the swabsticks may lead to contamination, compromising the sterility of the medical equipment and increasing infection risk.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients and healthcare providers must act quickly to avoid potential health risks associated with using contaminated products.
Practical Guidance
How to identify if yours is affected
- Check the SKU on the packaging: CIT6135B.
- Verify the lot number: 25EBC648.
- Stop using the product immediately if it matches the recalled items.
Where to find product info
The SKU and lot number can typically be found on the product packaging or the product box.
What timeline to expect
Allow 4-6 weeks for the refund process once the recalled kits are returned.
If the manufacturer is unresponsive
- Follow up with Medline Industries via phone or email.
- Document all communications with the company regarding the recall.
How to prevent similar issues
- Always check for seals and packaging integrity before using medical products.
- Stay informed about recalls in medical and healthcare products.
- Look for certifications indicating the product meets safety standards.
Documentation advice
Keep records of your purchase, including receipts and any correspondence with the manufacturer regarding the recall.
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Product Details
The recalled product is the MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B. It includes BD ChloraPrep Triple Swabsticks. The UDI/DI number is 10653160990666 and Lot Number is 25EBC648.
Key Facts
- Recall date: December 24, 2025
- Report date: February 18, 2026
- Quantity recalled: 168 units
- Open seal may compromise sterility
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Safety Guide
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