Medline recalls breast biopsy kits with specific lot numbers due to potential non-sterile solutions. This could lead to infection risks during medical procedures. Affected kits include those labeled BREAST BIOPSY KIT, REF MNS4360 with certain lot numbers.
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Medline is recalling breast biopsy kits that may contain non-sterile solutions, which could lead to infection risks during medical procedures. The recall affects kits with specific lot numbers and model references.
The kits were manufactured using specific lots of Nurse Assist products that may not be sterile. This could lead to non-sterile solutions being used during medical procedures, increasing the risk of infection.
Healthcare professionals using breast biopsy kits with the specified lot numbers and model references are most at risk. Patients undergoing procedures with these kits could face infection risks.
Check for kits labeled 'BREAST BIOPSY KIT, REF MNS4360' with lot numbers 2022091690, 2022112290, or 2022120990. The units have unique identifiers: case 10653160141716 and unit 00653160141719.
Look for the label 'BREAST BIOPSY KIT, REF MNS4360' and specific lot numbers on the packaging.
Medline is recalling these kits because the solutions used may not be sterile, which could lead to infection risks during medical procedures.
Lot numbers 2022091690, 2022112290, and 2022120990 are affected.
Check for kits labeled 'BREAST BIOPSY KIT, REF MNS4360' with the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1137-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1137-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
