Transpro Electric Scooters
Summary
CPSC recall: Transpro Electric Scooters. By Bike and electronics stores in the Northeast from August 2024 through April 2025 for between $250 and $400.. Hazard: The battery compartment of the recalled light-up ruler bracelets can be opened easily by children allowing access to the button cell batteries, violating the battery-operated toys requirements under the mandatory standard for toys. If a child swallows a button cell or coin battery, it can cause serious injuries, internal chemical burns o
Details
Source
CPSC Consumer Product Recall
External ID
10362
Action Date
2025-07-24
Status
Recalled
Category
consumer_product
Product Description
This recall involves Transpro brand A3 Hub Motor, A11F Spark, and R1 Commuter electric scooters. The scooters are powere
Context & Analysis
This is a unclassified recall.
This was one of 20 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 (Bike and electronics stores in the Northeast from August 2024 through April 2025 for between $250 and $400.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bike and electronics stores in the Northeast from August 2024 through April 2025 for between $250 and $400. have FDA actions?
This is the only FDA action we have on record for Bike and electronics stores in the Northeast from August 2024 through April 2025 for between $250 and $400. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10362" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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