Medline Industries recalled 117 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective tubing that may crack. Stop using these kits immediately and follow manufacturer instructions for return.
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 kits include various models such as the WATKINS SPINE PACK-LF and TOTAL HIP PACK, among others. They were manufactured and distributed nationwide in the U.S. The kits were sold under multiple SKUs, with a total of 117 units affected.
The MASTISOL liquid adhesive in these kits has been reported to cause the butyrate tubing to crack during use. This defect poses a risk of chemical exposure and potential complications during medical procedures.
No specific injuries have been reported at this time, but the potential for harm exists if the defective adhesive is used. The recall is classified as Class II, indicating a high hazard level.
Stop using the recalled kits immediately. Contact Medline Industries for further instructions on how to return the kits for a refund.
For inquiries, patients and healthcare providers can reach Medline Industries, LP. Visit the FDA recall page for more details at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1200-2026.
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