M.D.L. recalls aspirated biopsy needles with potential sterility issues. Affected models include PB1810 through PB2225. Consumers should contact M.D.L. for details.
Sterility assurance may be compromised.
M.D.L. is recalling aspirated cyto-histological biopsy needles due to possible sterility compromise. This could lead to infections if the needles are used improperly. The recall affects specific model numbers and production lots.
The needles may not maintain sterility properly, increasing the risk of infection during procedures. This could happen if the needles are contaminated after use or during handling.
Medical professionals and patients using the recalled biopsy needles. Those with the specific model numbers and production lots listed are most at risk.
Check the needle model number (PB1810 to PB2225) and production lot numbers (e.g., 1617A, 5216C) on the packaging or label.
Reach out to M.D.L. S.r.l. for specific instructions on how to handle the recalled needles.
The recall is due to potential sterility issues that could lead to infections if the needles are not properly maintained.
Models PB1810 through PB2225 with specific production lots like 1617A, 5216C, and 3620D.
Look for the model number and production lot on the needle packaging or label to match the affected models and lots listed.
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-2490-2021 — M.D.L. M.D.L. Hello, I own a M.D.L. that is covered by recall Z-2490-2021 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.
