Medline recalls 6 medical procedure kits with MASTISOL liquid adhesive that may crack during use, causing potential injury. Affected kits include DEPAUL BASIC NEURO-LF and NEURO MINOR models.
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.
Medline is recalling six medical procedure kits because the MASTISOL liquid adhesive inside them can crack during use. This crack risk could lead to injury if the adhesive leaks or causes contamination during medical procedures.
The MASTISOL liquid adhesive in these kits contains butyrate, which can crack during actuation (use) of the vials. If the tubing cracks, it may cause leaks or contamination during medical procedures, potentially leading to injury.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving care with these kits could also be affected if the adhesive cracks and leaks.
Check for kits labeled as DEPAUL BASIC NEURO-LF (SKU DYNJ20028L), NEURO MINOR (SKU DYNJ46546M), NEURO SHUNT PACK (SKU DYNJ54396K), NEURO PACK (SKU DYNJ59397Q), NEURO BASIC (SKU DYNJ904052L), or PK NEURO SHUNT BUMC (SKU DYNJT6428).
Look for the product name and SKU on the kit packaging to confirm if it matches the recalled models.
Medline is recalling these kits because complaints indicate the MASTISOL liquid adhesive can crack during use, which may cause leaks or contamination during medical procedures.
The recall record does not specify a remedy, so contact Medline directly for guidance on next steps.
The recall indicates a risk of cracked tubing during use, which could lead to leaks or contamination, but the record does not specify if this causes injury.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1196-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1196-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
