Medline recalls BILAT MICRO VASECTOMY REVERSAL kits with specific SKUs and lot numbers due to catheter surface finish and connector issues. Affected kits may have safety risks during medical procedures.
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 BILAT MICRO VASECTOMY REVERSAL. The kits have issues with catheter surface finish and connector detachment that could lead to safety problems during use.
The catheter surface finish irregularities and connector detachment issues could cause the catheter to malfunction during medical procedures. This might lead to complications if the catheter doesn't work as intended.
Medical professionals using the recalled kits for vasectomy reversals are most at risk. The recall affects specific kits sold with certain lot numbers and SKUs.
Check for the kit label 'BILAT MICRO VASECTOMY REVERSAL' and Medline SKU DYNJ68302. The affected kits have specific lot numbers listed in the recall notice.
Look for the label 'BILAT MICRO VASECTOMY REVERSAL' and Medline SKU DYNJ68302 on the kit.
Medline identified issues with catheter surface finish and connector detachment in some samples during an internal review.
The recall notice does not specify a remedy, so contact Medline directly for further instructions.
Affected lot numbers include 24CBL413, 24ABX694, 23JBY172, 23IBI716, 23DBG873, 23BBR326, 23ABH376, 22KBS634, 22JBS743, 22FBT429, 22BBZ842, 22BBK836, 21BBG579, 21ABO658.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2489-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2489-2026 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.
