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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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.
The recalled kits contain MASTISOL liquid adhesive, which has been reported to cause butyrate tubing to crack during use. This defect poses a significant risk to users of the medical kits.
Patients and healthcare providers should stop using the affected kits immediately. Contact Medline Industries for further instructions on returning the product and obtaining a refund.
For further assistance, contact Medline Industries, LP directly. Visit their website or call their customer service for more information.
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