Aesculap recalls 13 models of nonsterile hemostatic forceps due to breakage when used outside design specifications. Affected units include specific reference codes and GTINs.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap is recalling 13 different models of nonsterile hemostatic forceps because they can break when used in ways not covered by their design. This could lead to complications during medical procedures if the forceps fail unexpectedly.
The forceps can break when used in ways not intended by the manufacturer, such as applying excessive force or using them in situations beyond their design specifications. This breakage could cause complications during medical procedures if the forceps fail unexpectedly.
Medical professionals and surgical teams who use these forceps are most at risk. Patients undergoing procedures with these devices may face complications if the forceps break unexpectedly.
Check for reference codes like FB458R, FB459R, or FB738R on the packaging or product labels. Also look for GTIN numbers listed in the recall notice for each model.
Look for reference codes (e.g., FB458R) or GTIN numbers on the forceps packaging to confirm if your model is affected.
The recall states these forceps can break when used outside design specifications, so they are not safe for use in ways not covered by the manufacturer.
Check for reference codes like FB458R, FB459R, or FB738R on the packaging or product labels, and verify the GTIN numbers listed in the recall notice.
The recall does not specify a remedy, so you should check with Aesculap directly to determine next steps for affected units.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-1311-2025 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-1311-2025 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.
