Aesculap recalls specific surgical instruments due to potential insufficient sterilization in certain batches. Affected instruments may pose infection risks during procedures.
possibility of the sterility batch being insufficiently sterilized
Aesculap is recalling certain surgical instruments used in general and gynecologic procedures because some batches might not have been properly sterilized. This could lead to infection risks during surgery.
The instruments may not have been sufficiently sterilized, which could lead to infection if used during surgery. This is a potential risk in medical procedures where sterility is critical.
Surgical professionals using the recalled instruments in general or gynecologic procedures. The risk is primarily for those handling the specific lot numbers mentioned.
Check for the model 'CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM' with reference number PL730SU. Affected lots are 109C and 837B.
Look for the lot numbers 109C or 837B on the instrument packaging or label.
The recalled instrument is the CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM with reference number PL730SU.
This instrument is used in general surgery and gynecologic procedures where ligation and division of vessels is desired.
Check the lot number on the instrument. If it is 109C or 837B, contact Aesculap for further instructions.
We’ve drafted a message you can send Aescul: Aesculap Implant Systems LLC to request your refund or repair — edit it as you like.
Subject: Recall Z-2496-2019 — Aescul: Aesculap Implant Systems LLC Aescul: Aesculap Implant Systems LLC Hello, I own a Aescul: Aesculap Implant Systems LLC that is covered by recall Z-2496-2019 from Aescul: Aesculap Implant Systems LLC. 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.
