What should I do if I have one of the recalled Medline kits?

Stop using the recalled Medline kits immediately. Contact Medline Industries or your healthcare provider for specific instructions.

How can I find out if my Medline kit is affected by the recall?

Check the SKU on your Medline kit. The recalled kits are CATH LAB PACEMAKER PACK-LF (SKU DYNJ64837C) and LOOP RECOVERY PACK (SKU DYNJT7034).

Is there a refund or replacement for the recalled Medline kits?

Yes, patients and healthcare providers should follow the recall instructions provided by Medline for refunds or replacements.

What is MASTISOL and why is it dangerous in these kits?

MASTISOL is a liquid adhesive. The recall is due to issues with the tubing cracking during use, which can pose safety risks.

Where can I find more information about the recall?

Additional information can be found on the FDA's website at the provided recall notification page.

What are the symptoms of an issue with MASTISOL in these kits?

Symptoms may vary depending on the specific usage context, but any signs of malfunction or discomfort should prompt immediate consultation with a healthcare provider.

How long will it take to process my refund for the recalled kits?

The timeline for refunds can vary, but expect processing to take a few weeks after you follow the recall instructions.

Can I still use other Medline products that are not recalled?

Yes, if they are not part of this recall. Always check for any safety warnings or recalls before use.

What steps should I document regarding the recall?

Keep records of your communications with Medline, including any emails or notes from phone calls about the recall.

How can I file a complaint about the recalled product?

You can file a complaint with the FDA via their website for any safety concerns regarding the recalled product.

HIGHDecember 12, 2025

Medline Medical Kits Recalled Due to Liquid Adhesive Hazard

Medline Industries, LP recalled 1,928 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive linked to cracking tubing during use. Healthcare providers and patients must stop using these kits immediately.

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

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

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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.

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.

View Original Recall on FDA - Medical Devices

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Safety Guide

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Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH

Severity Score

8/ 10

Affected Groups

GENERAL

Injury Types

OTHER

Product Classification

CategoryHealth & Personal Care › Medical Devices

Product TypeMedical Procedure Convenience Kits

Product Details

Brand

Medline Industries, LP

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