M.D.L. recalls specific surgical instruments due to potential sterility compromise. Affected models and lot numbers listed; contact for remedy.
Sterility assurance may be compromised.
M.D.L. is recalling certain surgical instruments because they might not maintain sterility properly. This could lead to infections during medical procedures if used without proper cleaning.
The instruments may not maintain sterility during use, which could lead to infections if they are not properly cleaned or handled. This is a risk during medical procedures where sterility is critical.
Surgical staff and hospitals that use the recalled instruments. Patients at risk if the instruments are used without proper sterility.
Check for model numbers like MGC1413, MGP1410, or PM1410 with lot numbers 0817A, 5216C, or 3620D. These instruments were sold by M.D.L. in specific batches.
Identify the model number and lot number on the instrument to see if it matches the recalled list.
The instruments may not maintain sterility properly, which could lead to infections during medical procedures.
Check the model number and lot number on the instrument; affected models include MGC1413 with lot 0817A, and others listed in the recall notice.
The recall does not specify a remedy, so contact M.D.L. for guidance on next steps.
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-2493-2021 — M.D.L. M.D.L. Hello, I own a M.D.L. that is covered by recall Z-2493-2021 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.
