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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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.
The kits contain MASTISOL liquid adhesive. Complaints indicate that the butyrate tubing can crack during actuation, posing a risk to patients.
There are no specific reports of injuries or incidents associated with the use of these kits at this time. The nature of the hazard warrants immediate action to prevent potential risks.
Stop using the affected kits immediately. Contact Medline Industries, LP or your healthcare provider for further instructions on the recall process.
For more information, contact Medline Industries, LP at 1-800-396-2006 or visit their website. Further recall details are available at the FDA's enforcement report.
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