Aesculap Prestige Atraumatic Grasper Recall: Risk of Handle Separation

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Recalling firmAesculap Implant Systems LLC3773 Corporate Pkwy, N/A · Center Valley, PA 18034-8217

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Aesculap is recalling a specific type of endoscopic grasper that may separate at the weld between the handle and shaft. This could lead to the device becoming unusable or causing injury during medical procedures.

Why it’s dangerous

The handle and shaft of the grasper can separate at the weld during use, potentially causing the device to become detached. This could lead to the device being unusable or causing injury to the patient during surgery.

Who’s affected

Medical professionals using the Prestige Atraumatic Grasper during endoscopic procedures are most at risk. Patients receiving these devices as part of surgery may also be affected.

How to tell if you have this one

Check for product code 8360-10 and lot numbers listed in the description (M45041 through M55796). The device has a specific length (36cm) and diameter (5mm).

Brand
Aesculap
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Condition
Inspect the handle and shaft for separation at the weld. If separated, stop using the device immediately.

✎ GovInfoNow

Questions people ask

Why is this grasper being recalled?

The handle and shaft may separate at the weld during use, which could cause the device to become detached and potentially injure the patient.

What product codes are affected?

Product code 8360-10 with lot numbers M45041 through M55796.

How can I tell if I have the recalled grasper?

Look for the product code 8360-10 and lot numbers listed in the description (M45041 through M55796).

Take action

Contact Aesculap

We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1481-2022 — Aesculap Aesculap

Hello,

I own a Aesculap that is covered by recall Z-1481-2022 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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Where this comes from

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.

Official source: FDA Recall #Z-1481-2022 (April 1, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1481-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Aesculap Implant Systems LLC recalls PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10

Use caution until it’s fixed