Medline recalls baby admit procedural kits with plastic syringes that may leak or break, posing health risks. Affected kits include BABY ADMIT and BABY ADMIT KIT W/ PAMPERS models. Check pack numbers and lot numbers listed for your kit.
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 baby admit procedural kits that contain plastic syringes which may leak or break, potentially harming patients. This recall affects specific kits sold with certain pack numbers and lot numbers.
The plastic syringes in these kits can leak or break, which may lead to contamination or injury. This risk is particularly concerning for patient health during medical procedures.
Healthcare providers using these kits in hospitals or clinics are most at risk. Patients receiving care with these kits could be exposed to health hazards.
Check for kits labeled 'BABY ADMIT' or 'BABY ADMIT KIT W/ PAMPERS' with specific pack numbers like DYKB1011C or DYKB1011B. Also look for lot numbers such as 23ABQ306 or 22DBB502.
Look for the product name and pack number on the kit label to confirm if it's affected.
Reach out to Medline directly for assistance with the recall process.
The plastic syringes in these kits may leak or break, posing a risk to patient health.
Kits labeled 'BABY ADMIT' (pack numbers DYKB1011C) or 'BABY ADMIT KIT W/ PAMPERS' (pack numbers DYKB1011B) with listed lot numbers.
Check the product label for the specific pack number and lot number listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2757-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2757-2024 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.
