RecallHawk

CFMOTO ZFORCE 950 HO Sport Side-by-Side ROVs (2022-2023)

CFMOTO dealers nationwide from March 2022 through June 2024 for about $14,000.

Summary

CPSC recall: CFMOTO ZFORCE 950 HO Sport Side-by-Side ROVs (2022-2023). By CFMOTO dealers nationwide from March 2022 through June 2024 for about $14,000.. Hazard: The shock absorber rod assembly can unthread and detach, causing suspension collapse, posing crash and tip-over hazards to the rider.. Remedy: Consumers should immediately stop using the recalled ROVs, and contact an authorized CFMOTO dealer to schedule an appointment to bring the recalled vehicle into the dealer for a free repair. CFMO

Details

Source

CPSC Consumer Product Recall

External ID

10005

Action Date

2024-07-18

Status

Recalled

Category

consumer_product

Product Description

This recall involves 2022-2023 CFMOTO ZFORCE 950 HO Sport Side-by-Side Recreational Off Highway Vehicles sold in gray, o

Context & Analysis

This is a unclassified recall.

This was one of 11 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 (CFMOTO dealers nationwide from March 2022 through June 2024 for about $14,000.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does CFMOTO dealers nationwide from March 2022 through June 2024 for about $14,000. have FDA actions?

This is the only FDA action we have on record for CFMOTO dealers nationwide from March 2022 through June 2024 for about $14,000. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10005" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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