Medline recalls infant and obstetric delivery kits with specific pack numbers and lot numbers due to potential leaks and breakage 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 infant delivery kits and obstetric delivery kits that may leak or break, posing a risk to patient health. These kits contain plastic syringes affected by a recent FDA safety alert.
The plastic syringes in these kits may leak or break, which could lead to contamination or injury. This risk is identified by the FDA as a potential hazard during medical procedures involving patient care.
Healthcare providers using Medline procedural kits for infant or obstetric deliveries are most at risk. Patients receiving care with these kits could be affected if the kits leak or break.
Check for the product names: INFANT DELIVERY KIT (Pack Number DYKM1426) or SR OB DELIVERY (Pack Numbers DYNJ908583, DYNJ908583A, DYNJ909097). Also look for specific lot numbers listed in the recall notice.
Identify the pack number and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall is due to potential leaks and breakage in the plastic syringes, which could pose a risk to patient health as identified by the FDA Safety Alert from March 19, 2024.
The recall notice does not specify a remedy, so check the product details to see if your kit is affected and contact Medline for further instructions.
Yes, the recall includes specific lot numbers for each pack number, such as 21HME852 for DYKM1426.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2760-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2760-2024 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.
