Medline recalls convenience kits for breast biopsies with potential leaks and breakage that could harm patients. Affected kits include specific pack numbers 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 breast biopsy kits that may leak or break, posing a risk to patient health. These kits could cause injury if they malfunction during medical procedures.
The kits contain plastic syringes that can leak or break, potentially causing injury or infection during medical procedures. This risk is linked to FDA safety alerts about quality issues in these products.
Healthcare providers using these kits for breast biopsies are most at risk. Patients receiving procedures with these kits may face health hazards.
Check for pack numbers starting with DYNJ17400B, DYNJ32049A, DYNJ44987G, or DYNJ66288. Look for specific lot numbers listed in the recall notice.
Identify the pack number and lot number on the kit to confirm if it's affected by this recall.
Reach out to Medline for guidance on next steps if you have the recalled kits.
The kits contain plastic syringes that may leak or break, posing a risk to patient health as noted in an FDA safety alert.
Kits with pack numbers DYNJ17400B, DYNJ32049A, DYNJ44987G, or DYNJ66288 and specific lot numbers listed in the recall notice.
The recall does not require immediate stop use; healthcare providers should check details and contact Medline for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3003-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3003-2024 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.
