M.D.L. recalls specific bone marrow biopsy needles due to potential sterility issues. Affected models include PI1535/100, PIL1410/75, and others with listed lot numbers. Consumers should check their needle model and lot number to determine if it's affected.
Sterility assurance may be compromised.
M.D.L. is recalling certain bone marrow biopsy needles that may not maintain sterility, risking infection during medical procedures. This is serious because improper sterility could lead to infections in patients undergoing transplants.
The needles may not maintain sterility during use, which could lead to infections in patients undergoing bone marrow transplants. This is a critical risk because infections can be life-threatening for immunocompromised patients.
Patients receiving bone marrow transplants or their medical teams who use the recalled needles. Those with the specific model numbers and lot numbers listed are most at risk.
Check the needle model number (e.g., PI1535/100, PIL1410/75) and lot number (e.g., 3620D, 1617A) on the product packaging or label. The recall includes specific models and their associated lot numbers listed in the official notice.
Discontinue use of all recalled needles to prevent potential infection risks during medical procedures.
The recall includes needles with model numbers like PI1535/100, PIL1410/75, PIL1435/100, and others with specific lot numbers listed in the official notice.
Check the model number and lot number on your needle's packaging or label. Compare them to the list of affected models and lot numbers provided in the recall notice.
Immediately stop using the needles and contact your healthcare provider for guidance on safe alternatives or disposal.
We’ve drafted a message you can send M.D.L. to request your refund or repair — edit it as you like.
Subject: Recall Z-2489-2021 — M.D.L. M.D.L. Hello, I own a M.D.L. that is covered by recall Z-2489-2021 from M.D.L.. 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.
