Medline recalled multiple medical procedure convenience kits on December 12, 2025. The recall affects 66 units containing MASTISOL liquid adhesive. The adhesive's tubing may crack, posing a serious risk during use.
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's medical procedure convenience kits contain various surgical and medical supplies used in healthcare settings. Healthcare providers rely on these kits for quick access to necessary tools during procedures.
The recall involves MASTISOL liquid adhesive, whose tubing can crack during use, creating a risk of exposure. This defect can complicate medical procedures and lead to safety hazards for patients.
This recall is not part of a broader industry pattern.
Consumers must stop using the affected kits immediately, which could disrupt medical procedures and require alternatives.
The SKU and lot numbers are typically found on the packaging or the kit itself, near the barcode or product label.
Expect a refund or replacement to be processed within 4-6 weeks after your request.
Keep copies of all correspondence with Medline and any receipts associated with your purchase.
The recalled kits include the following models: MEM MAXILLOFACIAL PACK-LF (SKU DYNJ0660040R), PLASTICS VCH (SKU DYNJ39225K), WT BREAST PACK (SKU DYNJ46620I), ENDO / AUG PACK (SKU DYNJ59250I), KMC PLASTIC/GEN PACK-LF (SKU DYNJ65980J), PLASTICS PACK (SKU DYNJ68288A), IMPLANT REMOVAL KIT (SKU MNS13035), and PLASTICS PACK-LF (SKU PHS41746D). These kits were distributed nationwide.
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