RecallHawk

Summary

CPSC recall: Precor Resolute Cable Multi-Station Exercise Equipment. By The product was sold to fitness facilities nationwide from July 2023 through October 2024 for between $3,020 to $3,340 for the exercise station.. Hazard: The pop-pin can fail to fully engage in the exercise equipment's vertical rail and cause the pulley carriage to drop unexpectedly during use, posing an impact injury hazard to users.. Remedy: Consumers should immediately stop using the recalled exercise equipment. Precor is

Details

Source

CPSC Consumer Product Recall

External ID

10117

Action Date

2024-12-26

Status

Recalled

Category

consumer_product

Product Description

This recall involves Precor-branded Resolute Cable Multi-Station exercise equipment, Model No. RMS905, sold to gyms. The

Context & Analysis

This is a unclassified recall.

This was one of 8 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 (The product was sold to fitness facilities nationwide from July 2023 through October 2024 for between $3,020 to $3,340 for the exercise station.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does The product was sold to fitness facilities nationwide from July 2023 through October 2024 for between $3,020 to $3,340 for the exercise station. have FDA actions?

This is the only FDA action we have on record for The product was sold to fitness facilities nationwide from July 2023 through October 2024 for between $3,020 to $3,340 for the exercise station. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10117" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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