HIGHFDA DEVICE

Medline Medical Kits Recalled Due to Hazardous Adhesive

Medline recalled multiple medical procedure convenience kits on December 12, 2025. The recall affects 66 units containing MASTISOL liquid adhesive. The adhesive's tubing may crack, posing a serious risk during use.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesMedline Kit SKU DYNJ0660040R: UDI/DI 10889942220083 (EA) 40889942220084 (CS)Lot Number 25KMG652Medline Kit SKU DYNJ39225K: UDI/DI 10198459102257 (EA) 40198459102258 (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 DYNJ0660040R: UDI/DI 10889942220083 (EA) 40889942220084 (CS), Lot Number 25KMG652, Medline Kit SKU DYNJ39225K: UDI/DI 10198459102257 (EA) 40198459102258 (CS), Lot Number 25JMJ958, Lot Number 25KMJ566, Medline Kit SKU DYNJ46620I: UDI/DI 10198459404009 (EA) 40198459404000 (CS), Lot Number 25KBE927, Medline Kit SKU DYNJ59250I: UDI/DI 10198459359941 (EA) 40198459359942 (CS) +9 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's medical procedure convenience kits contain various surgical and medical supplies used in healthcare settings. Healthcare providers rely on these kits for quick access to necessary tools during procedures.

Why This Is Dangerous

The recall involves MASTISOL liquid adhesive, whose tubing can crack during use, creating a risk of exposure. This defect can complicate medical procedures and lead to safety hazards for patients.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers must stop using the affected kits immediately, which could disrupt medical procedures and require alternatives.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU number of your Medline kit against the list provided in the recall notice.
  2. Verify the lot number on your kit to ensure it is part of the recall.
  3. Contact Medline if you are uncertain about your kit's status.

Where to find product info

The SKU and lot numbers are typically found on the packaging or the kit itself, near the barcode or product label.

What timeline to expect

Expect a refund or replacement to be processed within 4-6 weeks after your request.

If the manufacturer is unresponsive

  • Follow up with Medline by phone or email.
  • Consider filing a complaint with the FDA if you do not receive a response.

How to prevent similar issues

  • Look for products with safety certifications when purchasing medical supplies.
  • Ask your healthcare provider about the safety records of the supplies they use.
  • Always verify recalls through official sources before using medical products.

Documentation advice

Keep copies of all correspondence with Medline and any receipts associated with your purchase.

Get instant alerts for Health & Personal Care recalls

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

No spamUnsubscribe anytime

Product Details

The recalled kits include the following models: MEM MAXILLOFACIAL PACK-LF (SKU DYNJ0660040R), PLASTICS VCH (SKU DYNJ39225K), WT BREAST PACK (SKU DYNJ46620I), ENDO / AUG PACK (SKU DYNJ59250I), KMC PLASTIC/GEN PACK-LF (SKU DYNJ65980J), PLASTICS PACK (SKU DYNJ68288A), IMPLANT REMOVAL KIT (SKU MNS13035), and PLASTICS PACK-LF (SKU PHS41746D). These kits were distributed nationwide.

Key Facts

  • Hazard due to MASTISOL adhesive
  • Manufactured by Medline Industries, LP
  • Stop using immediately

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
8/ 10
Affected Groups
GENERAL
Injury Types
BURNOTHER

Product Classification

Product Details

Model Numbers
Medline Kit SKU DYNJ0660040R: UDI/DI 10889942220083 (EA) 40889942220084 (CS)
Lot Number 25KMG652
Medline Kit SKU DYNJ39225K: UDI/DI 10198459102257 (EA) 40198459102258 (CS)
Lot Number 25JMJ958
Lot Number 25KMJ566
+12 more
Affected States
ALL
Report Date
February 4, 2026
Recall Status
ACTIVE

Related Recalls