Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    GUIDID: 04046955206742 Serial Numbers: 1004; 1026; 1032; 1035; 1036
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Aesculap Implant Systems LLC
Reason for Recall:
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010

Product Codes/Lot Numbers:

GUIDID: 04046955206742 Serial Numbers: 1004; 1026; 1032; 1035; 1036

Distribution:

Distributed in: US, AR, IN, NE, NC

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1516-2022

Related Recalls

Potential for the spring to become loose and fall out of the device, if the spring falls out during a surgical procedure, it may enter the patient's body.

Mar 21, 2023 Surgical Instruments Nationwide View Details →