Medline recalls procedural kits with plastic syringes that may leak or break, posing patient health risks. Affected kits include ultrasound catheter insertion and circumcision trays. Contact Medline for details.
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 procedural kits that contain plastic syringes prone to leaking or breaking, which could harm patients. This recall affects specific kits used for ultrasound catheter insertion and circumcision procedures.
The plastic syringes in these kits can leak or break, potentially causing patient health issues. This problem was identified through an FDA safety alert from March 19, 2024.
Healthcare providers using Medline procedural kits for ultrasound catheter insertion or circumcision procedures are most at risk. Patients receiving care from these kits may also be affected.
Check for kits labeled 'PERIPHERAL ULTRASOUND CATHETER INSERTION' with pack number MNS9865 or 'CIRCUMCISION' with pack numbers CIT6715 or CIT7095. Also look for specific lot numbers listed in the recall notice.
Look for the product names and pack numbers listed in the recall notice to confirm if your kit is affected.
Medline is recalling procedural kits labeled 'PERIPHERAL ULTRASOUND CATHETER INSERTION' (Pack Number MNS9865) and 'CIRCUMCISION' (Pack Numbers CIT6715 and CIT7095).
The plastic syringes in these kits may leak or break, posing a risk to patient health as identified by an FDA safety alert from March 19, 2024.
Check the labels on your kits for the specific pack numbers and lot numbers listed in the recall notice to determine if they 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-2742-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2742-2024 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.
