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 P903933B: UDI/DI 10889942362080 (EA) 40889942362081 (CS), Lot Number 25KMA871
- 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
February 11, 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
The Medline medical procedure convenience kits are designed for healthcare applications, providing necessary tools for procedures like shaving prior to surgery. Consumers typically purchase these kits for clinical settings where sterile procedures are required.
Why This Is Dangerous
The defect in the MASTISOL liquid adhesive kits is due to the butyrate tubing cracking, which can compromise the integrity of the adhesive and potentially expose users to harmful substances.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers should immediately stop using these kits to avoid potential exposure to unsafe materials. The recall could lead to inconvenience for healthcare providers who rely on these kits.
Practical Guidance
How to identify if yours is affected
- Check the SKU on the packaging: P903933B.
- Look for the Lot Number: 25KMA871.
- Verify if the kit is still in use.
Where to find product info
The SKU and Lot Number can typically be found on the product packaging or included in the user manual.
What timeline to expect
Expect 4-6 weeks for processing any refunds or replacements after contacting Medline.
If the manufacturer is unresponsive
- Contact Medline customer service again.
- Document all communications for reference.
- Consider reaching out to regulatory authorities if unresolved.
How to prevent similar issues
- Always check recall notices for medical supplies before purchase.
- Look for alternative brands with strong safety records.
- Ensure products are certified by regulatory agencies.
Documentation advice
Keep a record of your purchase, including receipts and any correspondence with the manufacturer regarding the recall.
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Product Details
The recalled product is the HEAD SHAVE-LATEX SAFE KIT, Kit SKU P903933B. The affected lot number is 25KMA871. These kits were distributed nationwide in the US.
Key Facts
- SKU P903933B affected
- Lot Number 25KMA871
- Stop using immediately
- Follow manufacturer 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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