Medline recalls 30+ medical procedure kits with MASTISOL liquid adhesive that cracks during use, potentially causing leaks. Affected kits include laparoscopy and abdominal endoscopy packs with specific SKUs and lot numbers.
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 30 different medical procedure kits that contain MASTISOL liquid adhesive which can crack during use. This crack risk may lead to leaks, though the record doesn't specify injuries or serious consequences.
The MASTISOL liquid adhesive in these kits can crack when activated, potentially causing leaks. This could lead to contamination or improper use during medical procedures, but the record doesn't mention injuries or serious harm.
Healthcare professionals using Medline medical procedure kits labeled with specific SKUs and lot numbers. Patients using these kits during procedures are at minimal risk if the kits are used properly.
Check for kits labeled with SKUs like DYNJ19974P, DYNJ20027K, or DYNJ20468J, and lot numbers starting with 25K (e.g., 25KMB830). The kits are used in medical procedures such as laparoscopy and abdominal endoscopy.
Look for specific SKUs and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall record mentions complaints about cracked tubing but does not specify any injuries or serious harm.
Check for kits with SKUs like DYNJ19974P, DYNJ20027K, or DYNJ20468J and lot numbers starting with 25K (e.g., 25KMB830).
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1191-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1191-2026 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.
