Medline Industries recalled 1,928 medical procedure convenience kits on December 12, 2025, due to a risk of crack in the adhesive tubing. The kits contain MASTISOL liquid adhesive, leading to safety concerns. Healthcare providers and patients should stop using the kits immediately and follow the 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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Medline medical procedure convenience kits are used in various healthcare settings for procedures that require sterile supplies. They include vital items necessary for patient care and treatment.
The kits contain MASTISOL liquid adhesive, which can cause the butyrate tubing to crack during use, leading to potential safety hazards for patients and healthcare providers.
This recall is not part of a broader industry pattern.
The recall affects healthcare providers and patients relying on these kits for medical procedures. Users must stop using the kits immediately, which may disrupt care and require alternative supplies.
The SKU and lot numbers are typically found on the product packaging or label.
Expect a refund or resolution within 4-6 weeks after returning the product.
Keep records of your purchase, any correspondence with Medline, and any medical documentation related to the use of the kit.
The recall involves two kits: INPATIENT CTRL LN DRG CHG (SKU DT22880) and ADULT CVC DRSG CHG W/ADHESIVE (SKU DYNDC3283A). These kits were distributed nationwide in the United States.
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