Medline recalls fetal surgery procedural kits with specific pack and lot numbers due to leaks and breakage risks that could harm patients during medical procedures.
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 fetal surgery procedural kits that may leak or break, posing risks to patient health. This affects kits with specific pack numbers and lot dates listed in the recall notice.
The kits contain plastic syringes that may leak or break, potentially causing contamination or injury to patients during medical procedures. This issue was identified after an FDA safety alert in March 2024.
Healthcare providers using Medline's fetal surgery kits are most at risk. Patients receiving procedures with these kits could face health issues if leaks or breakage occur.
Check for kits labeled 'FETAL SURGERY-LF' with pack number CDS840214Q or 'FETAL SURGERY CDS-LF' with pack numbers CMPJ26754O (lot 23HBE567) or CDS840214Q (lot 23IBC884).
Look for specific pack numbers and lot dates listed in the recall notice to confirm if your kit is affected.
The kits contain plastic syringes that may leak or break, posing risks to patient health as identified by an FDA safety alert in March 2024.
The recall notice does not specify a remedy, so check the kit labels for the specific pack numbers and lot dates to determine if your kit is affected.
Yes, leaks or breakage of the syringes could cause contamination or injury to patients during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2748-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2748-2024 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.