RecallHawk

Summary

CPSC recall: Electric Height-Adjustable Mobile Stands for Large Interactive Flat Panel Displays. By SMART authorized distributors and resellers who sold directly to businesses nationwide from May 2023 through December 2023 for about $1,735.. Hazard: The wheelbase welds on the stands can bend or break while the stand is being moved, causing the stands to fall over, posing tip-over and entrapment hazards.. Remedy: Consumers should immediately stop using the recalled mobile stands and contact SMART

Details

Source

CPSC Consumer Product Recall

External ID

9871

Action Date

2024-02-29

Status

Recalled

Category

consumer_product

Product Description

This recall involves SMART Technologies' Electric Height-Adjustable Mobile Stands for Large Interactive Flat Panel Displ

Context & Analysis

This is a unclassified recall.

This was one of 21 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (SMART authorized distributors and resellers who sold directly to businesses nationwide from May 2023 through December 2023 for about $1,735.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does SMART authorized distributors and resellers who sold directly to businesses nationwide from May 2023 through December 2023 for about $1,735. have FDA actions?

This is the only FDA action we have on record for SMART authorized distributors and resellers who sold directly to businesses nationwide from May 2023 through December 2023 for about $1,735. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9871" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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