Aesculap recalls laparoscopic trocar pins with possible sterility compromise due to damaged packaging. Affected units have product code EK236SU and batch numbers ending 12/08/2023. Consumers should check packaging for damage before use.
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 recall affects specific batch numbers produced in December 2023. The hazard is a potential loss of sterility, not a direct injury risk.
Damaged sterile packaging might allow contamination, leading to infection during surgery. The packaging is designed to maintain sterility until use, but if compromised, the pin could become unsterile.
Surgical teams using the recalled trocar pins for laparoscopic procedures are most at risk. Patients undergoing surgery with these pins could face infection if sterility is compromised.
Check for product code EK236SU on the packaging. The batch number ends with 52580815 and expires 12/08/2023. This product is used in laparoscopic procedures.
Inspect the sterile blister packaging for any signs of damage or compromise.
The recall states the packaging may be damaged, but if it appears undamaged, it may be safe. However, the manufacturer recommends checking for damage before use.
The recall does not specify a remedy, so you should check the packaging for damage before use. If damaged, do not use the product.
The batch number expires 12/08/2023, indicating production dates around December 2022.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-1246-2024 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-1246-2024 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.
