Medline recalls specific convenience kits for potential leaks and breakage that could harm patients. Affected kits include dialysis catheter insertion kits and angio packs with certain pack 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 several medical convenience kits due to reported leaks and breakage risks that could harm patients. These kits include dialysis catheter insertion kits and angio packs with specific pack and lot numbers. The issue may lead to patient health risks if the kits malfunction during use.
The kits contain plastic syringes that may leak or break, potentially causing patient harm. This risk is linked to quality issues identified by the FDA in March 2024.
Healthcare providers using the recalled Medline convenience kits are most at risk. Patients receiving procedures with these kits could be affected if the kits malfunction.
Check for kits labeled as Dialysis Catheter Insertion Kit (Pack CVI4815) or Angio Pack (Pack CVI5045) with specific lot numbers listed in the recall notice.
Look for the product name and pack number on the kit label to confirm if it matches the recalled items.
Reach out to Medline for guidance on next steps if you have the recalled kits.
The recall indicates potential leaks and breakage risks, so they should not be used until confirmed safe by Medline.
Dialysis Catheter Insertion Kits (Pack CVI4815) and Angio Packs (Pack CVI5045) with specific lot numbers listed in the recall.
Medline will provide guidance on replacements or remedies if you have the 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-2996-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2996-2024 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.
