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Medline Medical Procedure Kits Recalled Due to Tubing Hazard

Medline recalled 96 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective tubing that can crack during use. Patients and healthcare providers should stop using these products immediately.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesMedline Kit SKU DYNJ35494C: UDI/DI 10198459117879 (EA) 40198459117870 (CS)Lot Number 25KMD420Medline Kit SKU DYNJ38582O: UDI/DI 10198459603709 (EA) 40198459603700 (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
8/10

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 DYNJ35494C: UDI/DI 10198459117879 (EA) 40198459117870 (CS), Lot Number 25KMD420, Medline Kit SKU DYNJ38582O: UDI/DI 10198459603709 (EA) 40198459603700 (CS), Lot Number 25KMI679, Medline Kit SKU DYNJ82084F: UDI/DI 10198459089206 (EA) 40198459089207 (CS), Lot Number 25KMD145.
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 designed to assist healthcare providers during surgical procedures. These kits contain essential supplies, including adhesives, to ensure safe and effective operations.

Why This Is Dangerous

The recalled kits contain MASTISOL liquid adhesive with defective butyrate tubing that can crack during use, leading to potential complications during medical procedures.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

This recall affects healthcare providers and patients, requiring immediate cessation of use and potential disruption to medical procedures.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU number on the packaging of your Medline kits.
  2. Verify if your kit matches the affected SKUs: DYNJ35494C, DYNJ38582O, DYNJ82084F.
  3. Inspect for any visible damage to the packaging or contents.

Where to find product info

SKU numbers can typically be found on the packaging or the product label of the medical kits.

What timeline to expect

Expect a timeline of 4-6 weeks for refund processing after you submit your request.

If the manufacturer is unresponsive

  • Document all attempts to contact Medline.
  • Consider reaching out to your healthcare provider for assistance.

How to prevent similar issues

  • Look for products with safety certifications from recognized health organizations.
  • Verify the manufacturer's reputation for quality and safety before purchase.
  • Consult with healthcare professionals for recommendations on safe medical supplies.

Documentation advice

Keep receipts, correspondence, and any evidence of the product's condition for your records.

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Product Details

The recalled kits include the following: 1) C-SECTION PACK, Kit SKU DYNJ35494C; 2) SMJ C-SECTION PACK-LF, Kit SKU DYNJ38582O; 3) RR-L&D C-SECTION PACK-LF, Kit SKU DYNJ82084F. These kits were distributed nationwide in the U.S.

Key Facts

  • Recall date: December 12, 2025
  • 96 units recalled nationwide
  • Defective MASTISOL liquid adhesive
  • Immediate stop-use instructions issued

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
8/ 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 DYNJ35494C: UDI/DI 10198459117879 (EA) 40198459117870 (CS)
Lot Number 25KMD420
Medline Kit SKU DYNJ38582O: UDI/DI 10198459603709 (EA) 40198459603700 (CS)
Lot Number 25KMI679
Medline Kit SKU DYNJ82084F: UDI/DI 10198459089206 (EA) 40198459089207 (CS)
+1 more
Affected States
ALL
Report Date
February 4, 2026
Recall Status
ACTIVE

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