Medline recalls 70+ convenience kits with plastic syringes that may leak or break, posing health risks. Stop using immediately if you own these kits.
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 70 different medical convenience kits that contain plastic syringes affected by a recent FDA safety alert. These kits may leak or break, potentially causing health risks to patients. If you own any of these kits, stop using them immediately.
The plastic syringes in these kits have been identified by the FDA as having leaks, breakage, and other quality issues. These problems could lead to health risks for patients during medical procedures.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients using these kits for procedures may be affected if the syringes leak or break.
Check for kits labeled with specific names like ANGIOGRAPHY DRAPE PACK, CORONARY ANGIO PACK-LF, or other similar medical convenience kits. Look for the pack numbers listed in the recall notice, such as 00-401327AA, CDS780056K, etc.
If you own any of the recalled Medline convenience kits, stop using them right away to avoid potential health risks.
The recall includes 70 different medical convenience kits with specific names and pack numbers, such as ANGIOGRAPHY DRAPE PACK (Pack Number 00-401327AA) and CORONARY ANGIO PACK-LF (Pack Number 00-401594R).
Check the label on your kit for the specific product names and pack numbers listed in the recall notice, such as CDS780056K or VP SHUNT (Pack Number CDS840193U).
Stop using the kit immediately and do not use it for any medical procedures. The recall does not specify a return or replacement process.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3042-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3042-2024 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.
