Aesculap Caiman Articulating D5/360MM: Spring may fall out during surgery

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Contact the company & request your remedy

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Aesculap is recalling its Caiman Articulating D5/360MM surgical device because a spring could become loose and fall out during surgery, potentially entering the patient's body. This is a serious hazard that requires immediate attention from surgical teams using the device.

Why it’s dangerous

The device's spring can become loose and fall out during surgery. If it falls into the patient's body, it could cause injury or complications. This is a serious hazard that requires immediate action.

Who’s affected

Surgical teams using the Aesculap Caiman Articulating D5/360MM device for procedures like laparoscopic or arthroscopic surgery are most at risk. The hazard affects patients during surgery if the spring falls out.

How to tell if you have this one

Check for the product code PL771SU and lot number 52785146 on the device. The device is used for endoscopic surgery, including laparoscopic and arthroscopic procedures.

Brand
Aesculap
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using Device Now
Immediately stop using the Aesculap Caiman Articulating D5/360MM device if it has the product code PL771SU and lot number 52785146.

✎ GovInfoNow

Questions people ask

What is the product code for the recalled device?

The product code is PL771SU.

What lot number is associated with the recalled device?

The lot number is 52785146.

Is there a fix for this issue?

The recall record does not mention a fix or remedy.

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-1569-2023 — Aesculap Aesculap

Hello,

I own a Aesculap that is covered by recall Z-1569-2023 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-1569-2023 (March 21, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1569-2023 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 Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for

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