Aesculap recalls reducing converters (model EK087P) due to potential silicone fragments detaching from the yellow sealing component. Affected units sold between 2020-2023; contact for return.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Aesculap is recalling reducing converters that convert 10/12mm to 5mm sizes. Silicone fragments could detach from the yellow sealing part, posing a risk of injury if the fragments enter the body during use.
Silicone fragments may detach from the yellow sealing component during use. If these fragments enter the body, they could cause injury. However, the recall does not specify a mechanism for injury in normal use.
Users of medical-grade reducing converters for surgical procedures are most at risk. The product is used in medical settings, so healthcare professionals and surgical teams are the primary affected group.
Check for the model number EK087P on the converter. The product was sold between 2020 and 2023 with specific lot numbers listed in the recall notice.
Look for the model number EK087P on the converter to confirm if it is affected.
The recall states there is a potential for silicone fragments to detach, but it does not specify that the product is unsafe in normal use. Affected units should be checked for the model number.
The recall does not mention a replacement option; the remedy is null, meaning no specific action is required beyond checking if the product is affected.
The product was sold between 2020 and 2023, as indicated by the lot numbers listed in the recall notice.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-0312-2026 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-0312-2026 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.
