ProForm Rapid Strike 50 LB Adjustable Dumbbell Sets
Summary
CPSC recall: ProForm Rapid Strike 50 LB Adjustable Dumbbell Sets. By ProForm.com, Amazon.com, DicksSportingGoods.com, Lowes.com and Walmart.com from February 2021 through May 2024 for about $350.. Hazard: The weight plates can dislodge from the handle during use, posing an impact injury hazard.. Remedy: Consumers should immediately stop using the recalled ProForm Rapid Strike 50 LB Adjustable Dumbbell Sets, and contact iFIT to receive a free repair in the form of a replacement for the molded tra
Details
Source
CPSC Consumer Product Recall
External ID
10008
Action Date
2024-07-25
Status
Recalled
Category
consumer_product
Product Description
This recall involves the ProForm Rapid Strike 50 LB Adjustable Dumbbell Set, model PAMSDB20. The dumbbells were sold in
Context & Analysis
This is a unclassified recall.
This was one of 14 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 (ProForm.com, Amazon.com, DicksSportingGoods.com, Lowes.com and Walmart.com from February 2021 through May 2024 for about $350.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ProForm.com, Amazon.com, DicksSportingGoods.com, Lowes.com and Walmart.com from February 2021 through May 2024 for about $350. have FDA actions?
This is the only FDA action we have on record for ProForm.com, Amazon.com, DicksSportingGoods.com, Lowes.com and Walmart.com from February 2021 through May 2024 for about $350. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10008" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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