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 DYNJ64837C: UDI/DI 10198459139482 (EA) 40198459139483 (CS), Lot Number 25KMJ193, Medline Kit SKU DYNJT7034: UDI/DI 10198459592591 (EA) 40198459592592 (CS), Lot Number 25KMI766, .
- 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
April 13, 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
Medline medical procedure convenience kits are used in various healthcare settings for specific medical procedures. They are designed to provide essential items required during medical interventions.
Why This Is Dangerous
The kits contain MASTISOL liquid adhesive, which has been reported to crack the butyrate tubing during use. This defect can compromise the effectiveness of the adhesive and pose risks to patients.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall impacts healthcare providers and patients who rely on these convenience kits for safe medical procedures, creating urgency for immediate action.
Practical Guidance
How to identify if yours is affected
- Check the SKU on your Medline kit against the recalled list: DYNJ64837C and DYNJT7034.
- Look for the lot numbers: 25KMJ193 and 25KMI766 to verify your product.
- Contact your healthcare provider if you are unsure about the product's safety.
Where to find product info
The SKU and lot numbers can typically be found on the packaging or the kit itself.
What timeline to expect
Expect 4-6 weeks for refund processing after following the recall instructions.
If the manufacturer is unresponsive
- Follow up with Medline Industries via phone or email.
- Document all your communications for reference.
- Consider reaching out to the FDA if you receive no response.
How to prevent similar issues
- Always check for recalls before using medical products.
- Look for products with safety certifications when purchasing medical supplies.
- Consult healthcare professionals for guidance on medical supplies.
Documentation advice
Keep a record of your purchase, any correspondence with Medline, and the recall notice for your records.
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Product Details
The recall involves two Medline medical procedure convenience kits: 1) CATH LAB PACEMAKER PACK-LF, Kit SKU DYNJ64837C; 2) LOOP RECOVERY PACK, Kit SKU DYNJT7034. These kits were distributed nationwide in the U.S. as part of routine medical procedures.
Key Facts
- Recalled products: CATH LAB PACEMAKER PACK-LF and LOOP RECOVERY PACK
- Total units recalled: 1,928
- Recall date: December 12, 2025
- Contact Medline for instructions
- Nationwide distribution across the U.S.
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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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