Medline recalls 75+ medical procedure kits with plastic syringes that may leak or break, posing health risks. Affected kits include radial arterial line kits and PICC lines. Consumers should check product labels for 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 75 different medical procedure kits that contain plastic syringes which may leak or break. This could pose a risk to patient health during medical procedures.
The plastic syringes in these kits can leak or break, which may cause contamination or injury to patients during medical procedures. This risk is identified by the FDA Safety Alert from March 19, 2024.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients using these kits during procedures may be affected if the kits leak or break.
Check for kits labeled with pack numbers: ART240B, PICC0020, ART245B, SUT15940, or other specific pack numbers listed in the recall notice. Also look for lot numbers associated with these pack numbers.
Look for pack numbers and lot numbers on the kit labels to determine if your product is affected.
The recall states that these kits may leak or break, posing a risk to patient health. They should not be used until the recall is addressed.
Check the pack number and lot number on the kit. Affected kits include those with pack numbers like ART240B, PICC0020, ART245B, SUT15940, and others listed in the recall notice.
The recall does not specify a remedy, so contact Medline directly to get more information or instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2768-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2768-2024 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.
