🔍 RecallPedia

Navik 3D v2, REF NAVIK3D, 3D Mapping System

Class I - Dangerous
🏥 Medical Devices Recalled: November 7, 2023 APN Health Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI (01)00869781000308(11)180309(21)2UA7520XNT
  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:
APN Health LLC
Reason for Recall:
IFU update
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Navik 3D v2, REF NAVIK3D, 3D Mapping System

Product Codes/Lot Numbers:

UDI (01)00869781000308(11)180309(21)2UA7520XNT

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0556-2024