🔍 RecallPedia

EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi

Class I - Dangerous
🏥 Medical Devices Recalled: July 22, 2021 Philips Ultrasound Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Manufactured Between 2020-02-27 to 2021-05-25
  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:
Philips Ultrasound Inc
Reason for Recall:
Ultrasound system control panel arm swivel lock could fail, which could cause the control panel and monitor to swivel freely while a user is positioning the monitor, or transporting/moving the system, which could lead to patient or user musculoskeletal injury.
Classification:
Class I - Dangerous

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

Status:
completed

Product Information

Full Description:

EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi

Product Codes/Lot Numbers:

Manufactured Between 2020-02-27 to 2021-05-25

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2306-2021

Related Recalls

C6-2 Transducer Probe

Philips Ultrasound

Class I - Dangerous

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

Jul 3, 2025 Other Medical Devices Nationwide View Details →