Medline Industries recalls Centurion breast biopsy kits with specific pack numbers due to leaks and breakage risks that could harm patients during procedures.
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 Industries is recalling certain Centurion breast biopsy kits because they may leak or break, posing a risk to patient health. These kits are labeled with specific pack numbers and lots that could cause harm if used improperly.
The kits contain plastic syringes that may leak or break, potentially causing patient health issues during medical procedures. This risk is linked to quality issues identified by the FDA in March 2024.
Healthcare providers using these kits for breast biopsies are most at risk. Patients undergoing procedures with the recalled kits could face health issues due to leaks or breakage.
Check for kits labeled as 'BREAST BIOPSY KIT' with pack number MNS6950A or 'BREAST BIOPSY PACK' with pack number BT515A. Look for specific lot numbers listed in the recall notice.
Verify the pack number and lot number on the kit to determine if it is recalled.
The recall indicates potential leaks and breakage risks, so they are not safe to use without checking the specific pack numbers and lots.
Check the pack number and lot number on the kit to see if it matches the recalled items listed in the notice.
The recall notice does not mention a replacement option; the remedy is null.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-2771-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-2771-2024 from Medline Industries. 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.
