Medline recalls 72 convenience kits labeled with specific pack numbers and lot numbers due to potential leaks or breakage of plastic syringes that could pose a risk to patient health.
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 72 different convenience kits used in medical procedures because their plastic syringes may leak or break, which could pose a risk to patient health. These kits include items like angiography drapes and catheter packs. If you own any of these kits, you should 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 patient health risks if the syringes are used in medical procedures.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients using these kits during procedures may be exposed to health hazards if the syringes leak or break.
Check if your Medline convenience kit has a pack number listed in the recall (e.g., 00-398281J, 00-398650AG, etc.) and the corresponding lot number. The kits are used in medical procedures like angiography and catheter labs.
Immediately stop using any recalled Medline convenience kits with the listed pack numbers and lot numbers to avoid potential leaks or breakage of plastic syringes.
Medline is recalling 72 different convenience kits used in medical procedures because their plastic syringes may leak or break, which could pose a risk to patient health.
Check if your kit has a pack number listed in the recall (e.g., 00-398281J, 00-398650AG, etc.) and the corresponding lot number.
Immediately stop using the kit and contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2992-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2992-2024 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.
