Medline recalls medical procedure kits with specific lot numbers due to catheter surface finish and connector issues. Affected kits may have detachment risks or size problems.
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
Medline is recalling medical procedure kits labeled for Dr. Fernandez with specific kit numbers and lot numbers. The kits may have catheter surface finish irregularities, connector detachment issues, or incorrect outer diameter that could lead to medical complications during use.
The catheters in these kits may have surface finish irregularities, detach from the funnel prematurely, or be the wrong size. These issues could lead to medical complications during procedures if the kits are used as intended.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving care with these kits could face complications due to the catheter issues.
Check for the kit label with Dr. Fernandez's name and Medline kit number DYNJ68808. Look for lot numbers 21LBT965, 21IBU081, 21GBN159, or 21DBC976.
Look for the label with Dr. Fernandez's name and Medline kit number DYNJ68808.
Medline identified representative samples that didn't meet performance specifications, including catheter surface finish issues, connector detachment problems, and size discrepancies.
The recall record doesn't specify a remedy, so check the kit label and contact Medline for further instructions.
Yes, lot numbers 21LBT965, 21IBU081, 21GBN159, and 21DBC976 are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2498-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2498-2026 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.
