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 DYNJ0275635M: UDI/DI 10198459464799 (EA) 40198459464790 (CS), Lot Number 25KMH120, Medline Kit SKU DYNJ0395037X: UDI/DI 10198459600555 (EA) 40198459600556 (CS), Lot Number 25LMB119, Medline Kit SKU DYNJ04809N: UDI/DI 10198459440908 (EA) 40198459440909 (CS), Lot Number 25KMF969, Medline Kit SKU DYNJ0565499AN: UDI/DI 10195327318352 (EA) 40195327318353 (CS), Lot Number 25JMF339 +11 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 designed for use in various surgical procedures, providing essential tools and materials. Healthcare providers rely on these kits for efficiency and safety during surgeries.
Why This Is Dangerous
The defect in the MASTISOL adhesive causes the tubing to crack, which could lead to exposure to hazardous chemicals during procedures. This can result in complications for both patients and medical staff.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall poses a significant inconvenience for healthcare providers and patients, as it requires immediate cessation of use and returns. The safety of patients may be compromised if these defective kits are not addressed promptly.
Practical Guidance
How to identify if yours is affected
- Locate the SKU number on the kit packaging.
- Check the lot number against the recall list.
- Ensure the kit contains MASTISOL adhesive.
Where to find product info
Look for SKU and lot numbers on the outer packaging or instruction manual inside the kit.
What timeline to expect
Expect processing for returns to take about 4-6 weeks once initiated.
If the manufacturer is unresponsive
- Contact Medline customer service for updates.
- Document all interactions regarding the recall.
How to prevent similar issues
- Always verify product recalls before use.
- Look for FDA approval and safety certifications on medical devices.
- Choose kits with reputable brand histories.
Documentation advice
Keep records of your purchase, including receipts and correspondence with Medline regarding the recall.
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Product Details
The recalled kits include various models such as the WATKINS SPINE PACK-LF and TOTAL HIP PACK, among others. They were manufactured and distributed nationwide in the U.S. The kits were sold under multiple SKUs, with a total of 117 units affected.
Key Facts
- Contains MASTISOL liquid adhesive
- Defective tubing may crack
- Class II recall status
- Nationwide distribution in the U.S.
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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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