Medline Industries, LP recalled 857 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive which can cause butyrate tubing to crack during use. Healthcare providers and patients must stop using these kits immediately.
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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Medline medical procedure convenience kits are used in various healthcare settings to assist in surgical and medical procedures. These kits are typically purchased by hospitals and clinics for their convenience during operations.
The hazard arises from the MASTISOL liquid adhesive found in the kits. Complaints indicate that the butyrate tubing can crack during use, which may compromise the integrity of medical procedures.
This recall is not part of a broader industry pattern.
The recall creates a significant safety concern for healthcare providers and patients. Immediate action is necessary to prevent potential harm, and the inconvenience of returning products may affect medical operations.
The SKU numbers and UDI/DI numbers can be found on the product packaging or accompanying documentation.
Expect refund processing to take 4-6 weeks after your request is submitted.
Keep records of your purchase, including receipts and any correspondence related to the recall.
The recall affects 857 medical procedure convenience kits including various models such as DRAWER 1 AIRWAY Kit SKU ACC010270A and HYPOSPADIUS PACK Kit SKU DYNJ00282Q. These kits were distributed nationwide in the United States.
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