Quick Facts at a Glance
- Recall Date
- December 12, 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 Procedure Convenience Kits
- Model numbers
- Medline Kit SKU DYNJ16826O: UDI/DI 10195327412067 (EA) 40195327412068 (CS), Lot Number 25LMA655, Lot Number 25KMC911.
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 12, 2025
Reported by FDA DEVICE
February 4, 2026
RecallRadar source check
February 11, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
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 circumcision kit is designed for surgical procedures involving male circumcision. Healthcare providers use these kits for their convenience and sterile components.
Why This Is Dangerous
The hazard arises from the MASTISOL liquid adhesive, which can crack the butyrate tubing during use, potentially leading to contamination and adverse outcomes.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers must stop using these kits to avoid health risks associated with the adhesive failure. The inconvenience of returning the product and seeking alternatives may also affect healthcare providers.
Practical Guidance
How to identify if yours is affected
- Locate the SKU DYNJ16826O on the packaging.
- Check the lot numbers: 25LMA655 or 25KMC911.
- If your kit matches these identifiers, it is recalled.
Where to find product info
The SKU and lot numbers can be found on the external packaging of the kit or in the product documentation.
What timeline to expect
Expect a refund processing time of approximately 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Contact customer service again and document your communication.
- Reach out to regulatory bodies like the CPSC if the company does not respond.
How to prevent similar issues
- Always check for product recalls before using medical devices.
- Look for safety certifications when purchasing medical supplies.
- Be aware of recent recalls in the healthcare industry.
Documentation advice
Keep all correspondence with the manufacturer, including emails and notes from phone calls. Document any issues with the product, including photos if necessary.
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Product Details
The recalled product is labeled as CIRCUMCISION PACK, Kit SKU DYNJ16826O. The affected UDI/DI numbers are 10195327412067 for each kit and 40195327412068 for cases. Lot numbers include 25LMA655 and 25KMC911.
Key Facts
- Recalled 1,928 circumcision kits
- Manufactured by Medline Industries, LP
- Hazard due to MASTISOL liquid adhesive
- Stop using the product immediately
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Safety Guide
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