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 DT22880: UDI/DI 10653160995470 (EA) 40653160995471 (CS), Lot Number 25KMJ441, Medline Kit SKU DYNDC3283A: UDI/DI 10198459313240 (EA) 40198459313241 (CS), Lot Number 25KMH515.
- 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 for procedures that require sterile supplies. They include vital items necessary for patient care and treatment.
Why This Is Dangerous
The kits contain MASTISOL liquid adhesive, which can cause the butyrate tubing to crack during use, leading to potential safety hazards for patients and healthcare providers.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall affects healthcare providers and patients relying on these kits for medical procedures. Users must stop using the kits immediately, which may disrupt care and require alternative supplies.
Practical Guidance
How to identify if yours is affected
- Check the SKU on the kit packaging: DT22880 or DYNDC3283A.
- Verify the lot numbers: 25KMJ441 for SKU DT22880 or 25KMH515 for SKU DYNDC3283A.
- If the SKU matches, the kit is affected by the recall.
Where to find product info
The SKU and lot numbers are typically found on the product packaging or label.
What timeline to expect
Expect a refund or resolution within 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Document all communication attempts with Medline.
- Consider reaching out to the FDA for further assistance.
How to prevent similar issues
- Look for kits with well-reviewed adhesive alternatives.
- Check for recent recalls before purchase.
- Use products from reputable manufacturers with a strong safety record.
Documentation advice
Keep records of your purchase, any correspondence with Medline, and any medical documentation related to the use of the kit.
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Product Details
The recall involves two kits: INPATIENT CTRL LN DRG CHG (SKU DT22880) and ADULT CVC DRSG CHG W/ADHESIVE (SKU DYNDC3283A). These kits were distributed nationwide in the United States.
Key Facts
- Manufactured with MASTISOL liquid adhesive
- Stop using product immediately
- Contact Medline for instructions
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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