Medline Industries recalled 60 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive which has a defect causing butyrate tubing to crack. Users must stop using the kits immediately and follow recall instructions.
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.
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
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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.
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.
This recall is not part of a broader industry pattern.
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.
The SKU and Lot Number can typically be found on the product packaging or included in the user manual.
Expect 4-6 weeks for processing any refunds or replacements after contacting Medline.
Keep a record of your purchase, including receipts and any correspondence with the manufacturer regarding the recall.
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.
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