RecallHawk

Santa Cruz Bicycles 2022 Heckler 9 Electric Bicycles

Santa Cruz Bicycles LLC, of Santa Cruz, California

Summary

CPSC recall: Santa Cruz Bicycles 2022 Heckler 9 Electric Bicycles. By Santa Cruz Bicycles LLC, of Santa Cruz, California. Hazard: The latch mechanism that holds the battery in place can malfunction, causing the battery to dislodge from the frame and fall to the ground, posing a fall hazard to the rider. Additionally, the latch spring can cause additional wear on the battery housing over time, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled bicycles and contact

Details

Source

CPSC Consumer Product Recall

External ID

9303

Action Date

2022-05-05

Status

Recalled

Category

consumer_product

Product Description

This recall involves 2022 Santa Cruz Heckler 9 model electric bicycles (e-bikes), which were sold in Gloss Avocado Green

Context & Analysis

This is a unclassified recall.

This was one of 12 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Santa Cruz Bicycles LLC, of Santa Cruz, 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 (Santa Cruz Bicycles LLC, of Santa Cruz, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Santa Cruz Bicycles LLC, of Santa Cruz, California have FDA actions?

Santa Cruz Bicycles LLC, of Santa Cruz, 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 "9303" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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