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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 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 Kits
- Model numbers
- Medline Kit SKU DYNJ19974P: UDI/DI 10198459138195 (EA) 40198459138196 (CS), Lot Number 25KMB830, Lot Number 25KMB831, Medline Kit SKU DYNJ20027K: UDI/DI 10198459228957 (EA) 40198459228958 (CS), Lot Number 25KMG395, Lot Number 25KMH132, Medline Kit SKU DYNJ20468J: UDI/DI 10195327024338 (EA) 40195327024339 (CS), Lot Number 25KMF540 +10 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 12, 2025
Reported by FDA DEVICE
February 4, 2026
RecallRadar source check
April 13, 2026
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
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.
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
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
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 ProductGet Alerts for Health & Personal Care Recalls
Get instant alerts for recalls that affect you. Free forever.