Medline Industries recalled 456 medical procedure kits on December 12, 2025, due to a potential hazard involving MASTISOL liquid adhesive. The defective butyrate tubing may crack during use, posing a risk to patients and healthcare providers. Consumers must stop using these kits immediately and seek further 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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These medical procedure kits are used in various surgical operations and are essential for healthcare providers performing minimally invasive procedures. They contain necessary surgical tools and materials to facilitate surgeries.
The hazard arises from the MASTISOL adhesive, which may cause the butyrate tubing to crack during activation, potentially leading to exposure to harmful substances.
This recall is not part of a broader industry pattern.
The recall affects healthcare providers who rely on these kits for surgeries, creating potential delays in procedures and increased safety risks.
The SKU and lot numbers can typically be found on the packaging or accompanying documentation of the medical kits.
Expect a refund processing time of approximately 4-6 weeks after returning the product.
Keep records of your purchase, including receipts and any correspondence with the manufacturer regarding the recall.
The recall affects 456 units of various Medline surgical kits, including SMJ LAP CHOLE PACK-LF (SKU DYNJ19974P) and DEPAUL ABDOMINAL ENDOSCOPY-LF (SKU DYNJ20027K). These kits were distributed nationwide in the United States.
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