RecallHawk

Model Year 2024 Z Miami SE and Z Adventure Core Electric Bicycles

Super73 Inc., of Irvine, California

Summary

CPSC recall: Model Year 2024 Z Miami SE and Z Adventure Core Electric Bicycles. By Super73 Inc., of Irvine, California. Hazard: The retaining pin in the e-bike's disc brake calipers can loosen and dislodge from the caliper assembly, resulting in brake failure, posing crash and injury hazards to the rider.. Remedy: Consumers should immediately stop using the recalled e-bikes and contact the firm for a free repair kit. Consumers will receive a new retaining pin and up to $50 toward the cost of the

Details

Source

CPSC Consumer Product Recall

External ID

10174

Action Date

2025-02-20

Status

Recalled

Category

consumer_product

Product Description

This recall involves Super73's model year 2024 Z Miami SE (900-00288, 900-00309 and 900-00313) and Z Adventure Core (900

Context & Analysis

This is a unclassified recall.

This was one of 23 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Super73 Inc., of Irvine, California has 2 FDA actions in our database, including 1 recall.

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 (Super73 Inc., of Irvine, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Super73 Inc., of Irvine, California have FDA actions?

Super73 Inc., of Irvine, California has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10174" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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