Medline recalls surgical convenience kits with Pure Pouch components that have weak seals, risking sterility breaches. Affected kits include Cath Lab Special Procedure, Angiography, and Heart Catheterization packs with specific lot numbers and expiration dates.
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
Medline is recalling sterile surgical convenience kits that contain Pure Pouch components with weak seals. If the seal fails, the contents could become contaminated, posing a risk of infection during medical procedures.
The Pure Pouch components in these kits have weak seals that may fail, leading to breaches in sterility. This could allow contaminants to enter the surgical site, increasing infection risk during procedures.
Healthcare professionals using these surgical kits in medical facilities are most at risk. Patients undergoing procedures with these kits could face infection if sterility is compromised.
Check for specific pack numbers and lot numbers listed in the recall notice. Affected kits include Medline Cath Lab Special Procedure (Pack #00-RDF0360), Angiography (Pack #DYNJ26488W), and Heart Catheterization packs with the listed lot numbers and expiration dates.
Review the pack number and lot numbers on the kit to see if it matches the affected items listed in the recall notice.
The Pure Pouch components in these kits have weak seals that may fail, leading to breaches in sterility and potential infection risks during medical procedures.
Check the pack number and lot numbers on the kit against the list provided in the recall notice. Affected kits include specific Medline surgical packs with the listed lot numbers and expiration dates.
The recall notice does not specify a remedy, so contact Medline directly for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2224-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2224-2024 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.
