Medline Industries, LP recalled 1,928 circumcision procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive, which may 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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The recalled product is labeled as CIRCUMCISION PACK, Kit SKU DYNJ16826O. The affected UDI/DI numbers are 10195327412067 for each kit and 40195327412068 for cases. Lot numbers include 25LMA655 and 25KMC911.
The MASTISOL liquid adhesive in the kits has been reported to cause butyrate tubing to crack during actuation. This hazard poses a high risk of contamination and could lead to adverse medical effects.
No specific incidents or injuries related to this recall have been reported at this time. The recall follows complaints regarding the product's performance.
Patients and healthcare providers should stop using the kits immediately. Follow the recall instructions provided by Medline Industries, LP. Contact your healthcare provider for further instructions.
For additional information, consumers can contact Medline Industries, LP. Visit their website or contact them via email, fax, or telephone for guidance.
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