RecallHawk

American Angler Electric Fillet Knives

Weihai Yuanji Outdoor Products Co., Ltd. (RTI), of China

Summary

CPSC recall: American Angler Electric Fillet Knives. By Weihai Yuanji Outdoor Products Co., Ltd. (RTI), of China. Hazard: The trigger mechanism on the Electric Fillet Knife ("EFK") units can become stuck in the "on" position, posing a laceration hazard.. Remedy: Consumers should immediately stop using the recalled EFK, unplug the unit, and cut the power cord. Consumers should then contact Scott Fetzer Consumer Brands to receive a free replacement EFK by mail. Consumers will need to provide their

Details

Source

CPSC Consumer Product Recall

External ID

9198

Action Date

2021-12-29

Status

Recalled

Category

consumer_product

Product Description

This recall involves American Angler Electric Fillet Knives with model number 32300 and the following serial numbers: AE

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.

Weihai Yuanji Outdoor Products Co., Ltd. (RTI), of China 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 (Weihai Yuanji Outdoor Products Co., Ltd. (RTI), of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Weihai Yuanji Outdoor Products Co., Ltd. (RTI), of China have FDA actions?

Weihai Yuanji Outdoor Products Co., Ltd. (RTI), of China 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 "9198" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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