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 Convenience Kits
- Model numbers
- Medline Kit SKU ACC010270A: UDI/DI 10889942219827 (EA) 40889942219828 (CS), Lot Number 25LDA153, Medline Kit SKU ACC010690: UDI/DI 10195327433307 (EA) 40195327433308 (CS), Lot Number 25LDA088, Medline Kit SKU ACC011073: UDI/DI 10198459569333 (EA) 40198459569334 (CS), Lot Number 25LDA072, Medline Kit SKU DYNJ00282Q: UDI/DI 10195327412029 (EA) 40195327412020 (CS), Lot Number 25KMC904 +9 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
Medline medical procedure convenience kits are used in various healthcare settings to assist in surgical and medical procedures. These kits are typically purchased by hospitals and clinics for their convenience during operations.
Why This Is Dangerous
The hazard arises from the MASTISOL liquid adhesive found in the kits. Complaints indicate that the butyrate tubing can crack during use, which may compromise the integrity of medical procedures.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall creates a significant safety concern for healthcare providers and patients. Immediate action is necessary to prevent potential harm, and the inconvenience of returning products may affect medical operations.
Practical Guidance
How to identify if yours is affected
- Check the SKU numbers on your medical kits against the recall list.
- Look for the UDI/DI numbers on the packaging for identification.
- Contact your healthcare provider for assistance.
Where to find product info
The SKU numbers and UDI/DI numbers can be found on the product packaging or accompanying documentation.
What timeline to expect
Expect refund processing to take 4-6 weeks after your request is submitted.
If the manufacturer is unresponsive
- Follow up with Medline Industries through their customer service line or website.
- Document all communication attempts and keep records of your requests.
How to prevent similar issues
- When purchasing medical kits, ensure they meet current safety standards.
- Research the adhesive products used in medical devices for safety ratings.
- Always review recall notices for the latest product safety information.
Documentation advice
Keep records of your purchase, including receipts and any correspondence related to 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 857 medical procedure convenience kits including various models such as DRAWER 1 AIRWAY Kit SKU ACC010270A and HYPOSPADIUS PACK Kit SKU DYNJ00282Q. These kits were distributed nationwide in the United States.
Key Facts
- Manufactured by Medline Industries, LP
- Nationwide distribution in the U.S.
- Risk of cracked tubing during use
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.