Medline recalls neuro tray procedural kits with pack number DYNJ55909B due to potential leaks and breakage that could harm patient health. Affected kits may need replacement.
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 labeled 'NEURO TRAY' with pack number DYNJ55909B because they contain plastic syringes that can leak or break, posing a risk to patient health. This recall is important because medical devices that fail could lead to health issues during procedures.
The plastic syringes in these kits can leak or break, which may cause patient health issues during medical procedures. This risk arises from the quality issues identified in the FDA safety alert.
Healthcare professionals using Medline's neuro tray procedural kits with pack number DYNJ55909B are likely affected. Patients receiving care during procedures using these kits may be at risk if the kits malfunction.
Check for kits labeled 'NEURO TRAY' with pack number DYNJ55909B. The lot number for these kits is 23IBB122.
Look for the pack number DYNJ55909B and lot number 23IBB122 on the kit label.
The FDA safety alert identified leaks and breakage in the plastic syringes, which could pose a risk to patient health during procedures.
Check for kits labeled 'NEURO TRAY' with pack number DYNJ55909B and lot number 23IBB122.
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2759-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2759-2024 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.
