RecallHawk
Class II Recall

AMX Navigate Mobile X-Ray System

GE Healthcare, LLC

Summary

The FDA issued a Class II for AMX Navigate Mobile X-Ray System by GE Healthcare, LLC. Reason: An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system..

Details

Source

Device Recall

External ID

Z-2590-2021

Action Date

2021-10-06

Status

Terminated

Category

device

Product Description

AMX Navigate Mobile X-Ray System

Lot/Code Info: AMXNV2000001WK, AMXNV2000002WK, DF2401600003WK

Quantity Affected: 3 units

Reason for Recall

An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.

Distribution

Domestic Distribution Only

Type: Voluntary: Firm initiated

Recall Initiated: 2021-06-24

Company

GE Healthcare, LLC

Waukesha, WI

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 201 device recalls issued in the same week, part of 413 device-related FDA actions this month.

GE Healthcare, LLC has 104 FDA actions in our database, including 104 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GE Healthcare, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does GE Healthcare, LLC have FDA actions?

GE Healthcare, LLC has 104 FDA actions in our database, including 104 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-2590-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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