PlainRecalls
FDA Devices Low Class III Ongoing

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

Reported: December 20, 2023 Initiated: November 7, 2023 #Z-0556-2024

Product Description

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

Reason for Recall

IFU update

Details

Recalling Firm
APN Health LLC
Units Affected
1 unit
Distribution
US Nationwide distribution in the state of WI.
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
Navik 3D v2, REF NAVIK3D, 3D Mapping System. Recalled by APN Health LLC. Units affected: 1 unit.
Why was this product recalled?
IFU update
Which agency issued this recall?
This recall was issued by the FDA Devices on December 20, 2023. Severity: Low. Recall number: Z-0556-2024.