M.D.L. recalls specific soft tissue biopsy needles due to potential sterility compromise. Affected models and lot numbers listed. Consumers should check their items and contact the manufacturer for details.
Sterility assurance may be compromised.
M.D.L. is recalling certain soft tissue biopsy needles because they might not be sterile. This could lead to infections if used improperly. Affected items include specific models and lot numbers listed in the recall.
The needles may not be sterile, which could cause infections if used during medical procedures. This risk is specific to the recalled models and lot numbers.
Medical professionals and patients who use these needles for biopsies may be affected. Those with the listed models and lot numbers are most at risk.
Check the model number and lot number on the needle packaging. Affected models include MGK11210, MGK11410, and others listed with specific lot numbers.
Look for the model number and lot number on the needle packaging to see if it matches the recalled items.
The recall states sterility may be compromised, so they should not be used until the manufacturer confirms they are safe.
Check the model number and lot number against the list provided in the recall notice.
Contact M.D.L. directly to confirm if your needles are affected and follow their instructions.
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-2492-2021 — M.D.L. M.D.L. Hello, I own a M.D.L. that is covered by recall Z-2492-2021 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.
