Medline recalls specific circumcision procedure kits due to leaks and breakage risks that could harm patients. Affected kits include certain circumcision sets and trays with specific pack and lot numbers.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Medline is recalling specific circumcision procedure kits that contain plastic syringes prone to leaks and breakage. This poses a risk to patient health during medical procedures.
The plastic syringes in these kits can leak or break, potentially causing patient health issues. This risk is related to the FDA Safety Alert from March 19, 2024, which identified quality problems in the kits.
Healthcare providers using Medline circumcision kits with the listed pack and lot numbers are affected. Patients undergoing circumcision procedures with these kits may be at risk.
Check for circumcision sets labeled 'CIRCUMCISION SET' with pack number CIT6335 or circumcision trays with pack numbers listed in the recall notice. The specific lot numbers are also included in the recall.
Review the pack number and lot number on the kit to confirm if it matches the recalled items listed in the notice.
The kits contain plastic syringes that may leak or break, posing a risk to patient health as identified in the FDA Safety Alert from March 19, 2024.
Circumcision sets with pack number CIT6335 and specific circumcision trays with pack numbers including CIT6135BH, CIT2465, CIT4920, CIT7455, and others, along with their corresponding lot numbers.
Check the pack number and lot number on the kit to see if it matches the recalled items. If it does, contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2761-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2761-2024 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.
