Aesculap recalls 83 models of nonsterile hemostatic forceps due to breakage when used in ways not covered by design. Check product codes or GTINs for affected items.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap is recalling 83 different models of nonsterile hemostatic forceps because they can break when used in ways not intended by the design. This could lead to complications during medical procedures if the forceps break unexpectedly.
The forceps can break when used in ways not covered by the design, such as applying excessive force or using them in situations beyond their intended purpose. This breakage could cause complications during medical procedures.
Healthcare professionals and medical facilities that use these forceps for procedures are most at risk. Patients using these tools during surgery may face complications if the forceps break unexpectedly.
Check the product code (REF) listed in the recall notice, such as REF BH198R or REF BJ020R. Also look for the GTIN numbers provided for each model to identify affected items.
Identify the product code (REF) on the forceps, such as BH198R or BJ020R, to determine if it's affected.
The forceps have been used in ways not covered by the design, resulting in breakage of the clamps.
Check the product code (REF) on the forceps, such as BH198R or BJ020R, or look for the GTIN numbers listed in the recall notice.
The recall does not require stopping use; it only identifies models that can break when used in unintended ways.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-1310-2025 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-1310-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.