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Medline Medical Kits Recalled Over Hazardous Adhesive

Medline Industries recalled 236 medical procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive that may cause butyrate tubing to crack. Patients and healthcare providers should stop using these kits immediately.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesMedline Kit SKU DYNJ20028L: UDI/DI 10198459228995 (EA) 40198459228996 (CS)Lot Number 25LMA824Medline Kit SKU DYNJ46546M: UDI/DI 10198459526404 (EA) 40198459526405 (CS)

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
December 12, 2025
Status
ACTIVE
Severity
7/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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 DYNJ20028L: UDI/DI 10198459228995 (EA) 40198459228996 (CS), Lot Number 25LMA824, Medline Kit SKU DYNJ46546M: UDI/DI 10198459526404 (EA) 40198459526405 (CS), Lot Number 25KMH940, Medline Kit SKU DYNJ54396K: UDI/DI 10198459443138 (EA) 40198459443139 (CS), Lot Number 25KMD804, Medline Kit SKU DYNJ59397Q: UDI/DI 10198459495427 (EA) 40198459495428 (CS), Lot Number 25KMC287 +4 more
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 12, 2025

  2. Reported by FDA DEVICE

    February 4, 2026

  3. RecallRadar source check

    April 13, 2026

  4. 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 surgical and procedural applications. They are designed to provide essential tools and materials for medical professionals during patient care.

Why This Is Dangerous

The hazard arises from the MASTISOL liquid adhesive contained in the kits, which can cause the butyrate tubing to crack. This malfunction can lead to unsafe conditions during medical procedures, risking patient safety.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers using these kits should stop immediately and seek alternatives. The recall affects the availability of essential medical supplies, which may inconvenience healthcare providers.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU number on your kit against the recall notice.
  2. Look for lot numbers associated with the affected models.
  3. Verify if the kit was used during any medical procedures.

Where to find product info

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

What timeline to expect

Expect a refund or replacement processing time of about 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Follow up with Medline via phone or email.
  • Document all communications to ensure your inquiry is recorded.
  • Consider reaching out to regulatory bodies if you do not receive a response.

How to prevent similar issues

  • Always check for recalls on medical products before use.
  • Look for products with safety certifications from regulatory organizations.
  • Consider using alternative medical adhesives that have been verified as safe.

Documentation advice

Keep records of all communications, receipts, and any correspondence related to the recall for your documentation.

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Product Details

The recall includes the following kits: DEPAUL BASIC NEURO-LF (SKU DYNJ20028L), NEURO MINOR PACK (SKU DYNJ46546M), NEURO SHUNT PACK (SKU DYNJ54396K), NEURO PACK (SKU DYNJ59397Q), NEURO BASIC (SKU DYNJ904052L), PK NEURO SHUNT BUMC (SKU DYNJT6428). These kits were distributed nationwide.

Key Facts

  • Hazard due to MASTISOL adhesive
  • Immediate action required
  • Contact Medline for instructions

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

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeMedical Procedure Convenience Kits
Sold At
Multiple Retailers

Product Details

Model Numbers
Medline Kit SKU DYNJ20028L: UDI/DI 10198459228995 (EA) 40198459228996 (CS)
Lot Number 25LMA824
Medline Kit SKU DYNJ46546M: UDI/DI 10198459526404 (EA) 40198459526405 (CS)
Lot Number 25KMH940
Medline Kit SKU DYNJ54396K: UDI/DI 10198459443138 (EA) 40198459443139 (CS)
+7 more
Affected States
ALL
Report Date
February 4, 2026
Recall Status
ACTIVE

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