NordicTrack 50 LB iSelect Voice-Controlled Adjustable Dumbbells
Summary
CPSC recall: NordicTrack 50 LB iSelect Voice-Controlled Adjustable Dumbbells. By NordicTrack.com, Amazon.com and DicksSportingGoods.com from January 2022 through November 2023 for between $500 and $600.. Hazard: The weight plates can dislodge from the handle during use, posing an impact hazard.. Remedy: Consumers should immediately stop using the recalled NordicTrack 50 LB iSelect Voice-Controlled Adjustable Dumbbells and contact iFIT to receive a full refund. iFIT is contacting all known purcha
Details
Source
CPSC Consumer Product Recall
External ID
9839
Action Date
2024-02-01
Status
Recalled
Category
consumer_product
Product Description
This recall involves the iFIT NordicTrack 50 LB iSelect Voice-Controlled Adjustable Dumbbells, model NTSAW23020.0. The d
Context & Analysis
This is a unclassified recall.
This was one of 18 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 (NordicTrack.com, Amazon.com and DicksSportingGoods.com from January 2022 through November 2023 for between $500 and $600.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does NordicTrack.com, Amazon.com and DicksSportingGoods.com from January 2022 through November 2023 for between $500 and $600. have FDA actions?
This is the only FDA action we have on record for NordicTrack.com, Amazon.com and DicksSportingGoods.com from January 2022 through November 2023 for between $500 and $600. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9839" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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