What should I do if I have a recalled Medline kit?

Stop using the recalled Medline kits immediately. Follow the instructions provided by Medline Industries for returning the kits.

What is the hazard associated with the recalled Medline kits?

The hazard involves the MASTISOL liquid adhesive, which may cause the butyrate tubing to crack, posing a risk during medical procedures.

How can I identify if my Medline kit is affected?

Check for any of the listed SKUs, like WATKINS SPINE PACK-LF or TOTAL HIP PACK, and ensure the lot numbers match those provided in the recall.

Will I receive a refund for the recalled product?

Yes, you should receive a refund as part of the recall process. Contact Medline for specific instructions.

Where can I find more information on the recall?

Visit the FDA recall page at the provided URL for detailed information and guidance.

What if I experience issues while using the Medline kit?

If you experience any issues, contact your healthcare provider immediately. Report any adverse reactions to Medline and the FDA.

Are there any injuries reported from these kits?

As of now, there are no specific injuries reported; however, the potential for harm exists.

How long will it take to process my return?

Processing time for returns typically takes about 4-6 weeks.

Can I still use the Medline kits if they look fine?

No, do not use the kits even if they appear undamaged due to the potential hazards.

What are chemical hazards in medical devices?

Chemical hazards refer to risks posed by substances, such as adhesives, in medical devices that can cause adverse reactions or complications.

HIGHDecember 12, 2025

Medline Recalls Medical Kits Due to Adhesive Tubing Hazard

Medline Industries recalled 117 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective tubing that may crack. Stop using these kits immediately and follow manufacturer instructions for return.

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 designed for use in various surgical procedures, providing essential tools and materials. Healthcare providers rely on these kits for efficiency and safety during surgeries.

Why This Is Dangerous

The defect in the MASTISOL adhesive causes the tubing to crack, which could lead to exposure to hazardous chemicals during procedures. This can result in complications for both patients and medical staff.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall poses a significant inconvenience for healthcare providers and patients, as it requires immediate cessation of use and returns. The safety of patients may be compromised if these defective kits are not addressed promptly.

Practical Guidance

How to identify if yours is affected

Locate the SKU number on the kit packaging.
Check the lot number against the recall list.
Ensure the kit contains MASTISOL adhesive.

Where to find product info

Look for SKU and lot numbers on the outer packaging or instruction manual inside the kit.

What timeline to expect

Expect processing for returns to take about 4-6 weeks once initiated.

If the manufacturer is unresponsive

Contact Medline customer service for updates.
Document all interactions regarding the recall.

How to prevent similar issues

Always verify product recalls before use.
Look for FDA approval and safety certifications on medical devices.
Choose kits with reputable brand histories.

Documentation advice

Keep records of your purchase, including receipts and correspondence with Medline regarding the recall.

Product Details

The recalled kits include various models such as the WATKINS SPINE PACK-LF and TOTAL HIP PACK, among others. They were manufactured and distributed nationwide in the U.S. The kits were sold under multiple SKUs, with a total of 117 units affected.

Key Facts

117 units recalled
Contains MASTISOL liquid adhesive
Defective tubing may crack
Class II recall status
Nationwide distribution in 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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