Medline Industries, LP recalled 1,928 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive linked to cracking tubing 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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The recall involves two Medline medical procedure convenience kits: 1) CATH LAB PACEMAKER PACK-LF, Kit SKU DYNJ64837C; 2) LOOP RECOVERY PACK, Kit SKU DYNJT7034. These kits were distributed nationwide in the U.S. as part of routine medical procedures.
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 patients relying on these medical kits.
There have been multiple complaints regarding the MASTISOL liquid adhesive leading to tubing cracks. The exact number of injuries or adverse events reported is not specified.
Healthcare providers and patients should immediately stop using the affected kits. Contact Medline Industries or your healthcare provider for further instructions regarding the recall.
For further assistance, contact Medline Industries, LP at their official website or through their customer service. Additional information is available on the FDA's recall notification page.
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