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

Stop using the recalled kits immediately. Follow the instructions provided by Medline or your healthcare provider for returning the products.

What is the hazard associated with the Medline kits?

The kits contain MASTISOL liquid adhesive, which may cause the butyrate tubing to crack, posing a risk of exposure to hazardous materials.

How can I identify if my Medline kit is affected by this recall?

Check the SKU numbers listed in the recall announcement. Affected kits include various SKUs such as DYNJ19974P and DYNJ20027K.

Where can I find more information about the recall?

More information can be found on the FDA's website, or by contacting Medline Industries directly.

Is there a risk of injury associated with using these kits?

While there have been no reported injuries, the potential for hazardous exposure exists. It is recommended to stop using the kits immediately.

How will Medline notify consumers about the recall?

Medline will notify consumers via email, fax, letter, press release, telephone, or visits.

What is the classification of this recall?

This recall is classified as Class II, indicating that the use of the recalled product may cause temporary or medically reversible adverse health consequences.

Can I return the recalled kits without a receipt?

Yes, consumers have the right to a full refund regardless of whether they have the receipt.

What if I experience symptoms after using a recalled kit?

If you experience any symptoms after using a recalled kit, seek medical attention immediately and report the incident to your healthcare provider.

How long will it take to process a refund for the recalled product?

Refund processing typically takes about 4-6 weeks, depending on the company's policies.

HIGHDecember 12, 2025

Medline Medical Procedure Kits Recalled Over Adhesive Hazard

Medline Industries recalled 456 medical procedure kits on December 12, 2025, due to a potential hazard involving MASTISOL liquid adhesive. The defective butyrate tubing may crack during use, posing a risk to patients and healthcare providers. Consumers must stop using these kits immediately and seek further instructions.

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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

About This Product

These medical procedure kits are used in various surgical operations and are essential for healthcare providers performing minimally invasive procedures. They contain necessary surgical tools and materials to facilitate surgeries.

Why This Is Dangerous

The hazard arises from the MASTISOL adhesive, which may cause the butyrate tubing to crack during activation, potentially leading to exposure to harmful substances.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall affects healthcare providers who rely on these kits for surgeries, creating potential delays in procedures and increased safety risks.

Practical Guidance

How to identify if yours is affected

Check the SKU number on your medical procedure kit against the recalled list.
Look for the UDI/DI numbers on the packaging.
Verify the lot numbers provided in the recall announcement.

Where to find product info

The SKU and lot numbers can typically be found on the packaging or accompanying documentation of the medical kits.

What timeline to expect

Expect a refund processing time of approximately 4-6 weeks after returning the product.

If the manufacturer is unresponsive

Contact Medline Industries directly through their customer service line.
Document your correspondence and keep records of your communication.

How to prevent similar issues

When purchasing medical kits, check for safety certifications and recalls.
Ensure that the supplier provides clear labeling and product information.
Consider alternatives with established safety records.

Documentation advice

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

Product Details

The recall affects 456 units of various Medline surgical kits, including SMJ LAP CHOLE PACK-LF (SKU DYNJ19974P) and DEPAUL ABDOMINAL ENDOSCOPY-LF (SKU DYNJ20027K). These kits were distributed nationwide in the United States.

Key Facts

Recall Date: December 12, 2025
Report Date: February 4, 2026
Total Units Recalled: 456
Affected Products: Various Medline surgical kits
Hazard: Cracked tubing in MASTISOL adhesive

View Original Recall on FDA - Medical Devices

Browse More Recalls

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH

Severity Score

7/ 10

Affected Groups

GENERAL

Injury Types

OTHER

Product Classification

CategoryHealth & Personal Care › Medical Devices

Product TypeMedical Procedure Kits

Product Details

Brand

Medline Industries, LP

Related Recalls

Health & Personal Care

HIGH

Medline Angiography Kit Recall: 3,120 Medical Convenience Kits With NAMIC Adaptor May Disconnect (Z-

Medline Industries, LP recalls 3,120 medical convenience kits worldwide due to a risk the syringe rotating adaptor may unwind during use. The issue can create a loose connection or complete disconnection between the syringe and manifold. The recall was issued on February 27, 2026 and is active. Customers should stop using the kit and follow manufacturer instructions for recall notices.

Feb 27, 2026

Medline Industries, LP

Medline Industries,

Health & Personal Care

HIGH

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in Class I Action for 79,843 Units

Medline Industries issued a Class I recall for 79,843 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The action covers worldwide distribution including the US and PR. The risk is a syringe adaptor unwinding during use, which may cause a loose connection or disconnection with the manifold. Stop using the device immediately and follow recall instructions.

Feb 27, 2026

Medline Industries, LP

Medline Industries,

Health & Personal Care

HIGH

Medline Angiographic Control Syringe Recall for 192,690 Units Over Rotating Adaptor Hazard (2026)

Medline Industries recalls 192,690 Angiographic Control Syringes worldwide after post-market surveillance found a rotating adaptor may unwind. The defect can cause a loose or complete disconnection between syringe and manifold. Stop using immediately and follow recall instructions.

Feb 27, 2026

Medline Industries, LP

Medline Industries,

Health & Personal Care

HIGH

Medline NAMIC Angiographic Syringe Recall Affects 17,902 Kits Worldwide (2026)

Medline Industries, LP recalls 17,902 medical convenience kits worldwide after post-market surveillance found a potential risk of the syringe rotating adaptor unwinding. The recall covers NAMIC Angiographic RA control syringes labeled in 10 Medline SKUs. Healthcare providers should stop use immediately and follow recall instructions.

Feb 27, 2026

Medline Industries, LP

Medline Industries,

Health & Personal Care

HIGH

Medline NAMIC Angiographic Rotating Adaptor Syringe Recall Affects 762 Units Worldwide (2026)

Medline Industries, LP recalls 762 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes sold worldwide, including the U.S., PR, Canada, and several international markets. The recall cites a potential risk that the syringe rotating adaptor may unwind during use, creating a loose connection or disconnect between the syringe and the manifold. Stop using the device and seek

Feb 27, 2026

Medline Industries, LP

Medline Industries,

Health & Personal Care

HIGH

Medline NAMIC Angiographic Adaptor Syringes Recalled in 439 Kits for Unwind Risk (2026)

Medline Industries, LP recalled 439 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans worldwide distribution including the US, Puerto Rico, and multiple international markets.

Feb 27, 2026

Medline Industries, LP

Medline Industries,

Health & Personal Care

HIGH

Medline NAMIC RA Syringe Adaptor Recall Aims to Prevent Connection Failures in 60 Kits (2026)

Medline Industries, LP recalled 60 medical convenience kits worldwide due to a potential rotating adaptor unwinding in NAMIC Angiographic RA control syringes. The issue may cause a loose connection or disconnection between the syringe and manifold. Healthcare providers should stop using the device and follow the manufacturer’s recall instructions.

Feb 27, 2026

Medline Industries, LP

Medline Industries,

Health & Personal Care

HIGH

Medline NAMIC Angiographic RA Syringes Recalled in 1698 Kits for Unwinding Adaptor Risk (2026)

Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.

Feb 27, 2026

Medline Industries, LP

Medline Industries,