Aesculap recalls laparoscopic trocar pins with possible sterility compromise due to damaged blister packaging. Affected units include Product Code EK234SU with batch 52573073 expiring 12/08/2023.
The sterile blister packaging may be damaged, and sterility may be compromised.
Aesculap is recalling laparoscopic trocar pins that may have damaged sterile packaging, risking infection during surgery. This affects specific batch numbers sold between 2021 and 2023.
Damaged blister packaging could allow contamination, potentially leading to surgical site infections. The risk is related to the packaging integrity, not the device itself.
Surgical teams using the recalled trocar pins for laparoscopic procedures. Patients undergoing surgery with these pins are at risk of infection if sterility is compromised.
Check for Product Code EK234SU on the packaging. The batch number 52573073 expires on 12/08/2023. These pins were sold for laparoscopic procedures between 2021 and 2023.
Inspect the blister packaging for damage or signs of contamination before use.
The recall indicates potential sterility risks from damaged packaging, so it's not recommended for use until verified.
The recall does not specify a remedy, so check packaging for damage and contact Aesculap for guidance.
Look for Product Code EK234SU with batch number 52573073 expiring 12/08/2023.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-1245-2024 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-1245-2024 from Aesculap. 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.
