🔍 RecallPedia

Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software

Class I - Dangerous
🏥 Medical Devices Recalled: June 26, 2023 Digisonics Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    UDI?DI 00857050006014, Versions 4.8.2 SP6 - 4.8.3
  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:
Digisonics, Inc
Reason for Recall:
Software issue
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software

Product Codes/Lot Numbers:

UDI?DI 00857050006014, Versions 4.8.2 SP6 - 4.8.3

Distribution:

Distributed in: US, AK, NH, WY, TX, NE, CA, MD, OR, IA, IL, MO, NY, UT, PA, MA, GA, VA, WA, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2214-2023