Aesculap recalls 18 models of nonsterile hemostatic forceps due to risk of clamp breakage during use. Affected models include REF BJ500R to REF MD592 with specific GTIN numbers.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap has recalled 18 different models of nonsterile hemostatic forceps because they can break during use. This breakage could cause injury if the forceps are used in medical procedures. Affected users should check their product details against the list provided.
The forceps can break when used in ways not covered by their design, such as during certain surgical procedures. This breakage may lead to complications if the forceps are not properly secured or if they fail unexpectedly during use.
Medical professionals and surgical staff who use these forceps are most at risk. Patients undergoing surgery with these specific models could be affected if the forceps break during procedures.
Check for model numbers starting with REF BJ500R through REF MD592. Look for the specific GTIN numbers listed in the recall notice to confirm if your forceps are affected.
Compare your forceps model and GTIN numbers with the list of affected items provided in the recall notice.
The recall indicates a risk of breakage during use, so affected models should not be used until the recall is addressed.
Check if your forceps model starts with REF BJ500R through REF MD592 and matches the specific GTIN numbers listed in the recall notice.
Contact Aesculap directly to confirm your model and follow their instructions for safe handling or replacement.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-1308-2025 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-1308-2025 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.
