Medline recalls 15 types of convenience kits with plastic syringes that may leak or break, posing health risks. Affected kits include EP DRAPE PACK-LF and MERCY COMBINED PACK-LF models with specific pack numbers and lot numbers.
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 15 different medical convenience kits that contain plastic syringes which may leak or break. This could pose a risk to patient health if the kits are used improperly.
The plastic syringes in these kits have been identified by the FDA as having leaks, breakage, or other quality issues. These problems could lead to patient health risks if the syringes are used during medical procedures.
Healthcare professionals and medical facilities that use these convenience kits are most at risk. Patients using the kits for medical procedures may be affected if the syringes leak or break.
Check for kits labeled as EP DRAPE PACK-LF or MERCY COMBINED PACK-LF with specific pack numbers listed in the recall notice. The kits have unique pack numbers and lot numbers that are detailed in the recall.
Look for the product name and pack number on the kit label to determine if it is affected.
The recall states that the plastic syringes may leak or break, posing a risk to patient health. Affected kits should not be used until the recall is addressed.
Check the product name and pack number on the kit label. Affected kits include EP DRAPE PACK-LF and MERCY COMBINED PACK-LF with specific pack numbers listed in the recall notice.
The recall does not specify a remedy, so contact Medline directly for guidance on how to handle affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3037-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3037-2024 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.
