RecallHawk

YTL Log Splitters with Briggs & Stratton 250cc engines

Briggs & Stratton, of Wauwatosa, Wis. (engine)

Summary

CPSC recall: YTL Log Splitters with Briggs & Stratton 250cc engines. By Briggs & Stratton, of Wauwatosa, Wis. (engine). Hazard: An incorrect engine ignition coil and flywheel can lead to hard starting and engine kick back, posing an injury hazard to the operator.. Remedy: Consumers should immediately stop using the recalled log splitters and contact an authorized Briggs & Stratton dealer for a free inspection and repair. Briggs & Stratton is contacting all purchasers directly..

Details

Source

CPSC Consumer Product Recall

External ID

9022

Action Date

2021-03-18

Status

Recalled

Category

consumer_product

Product Description

The recall involves YTL log splitters powered by Briggs & Stratton 250cc engine, with engine model number 15T232-0011-F8

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.

Briggs & Stratton, of Wauwatosa, Wis. (engine) has 4 FDA actions in our database, including 2 recalls.

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 (Briggs & Stratton, of Wauwatosa, Wis. (engine)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Briggs & Stratton, of Wauwatosa, Wis. (engine) have FDA actions?

Briggs & Stratton, of Wauwatosa, Wis. (engine) has 4 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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