RecallHawk

U-Line Outdoor Series 24-inch Built-In Convertible Freezers

U-Line Corporation, of Milwaukee, Wisconsin

Summary

CPSC recall: U-Line Outdoor Series 24-inch Built-In Convertible Freezers. By U-Line Corporation, of Milwaukee, Wisconsin. Hazard: The outdoor freezers can overheat, posing a fire hazard.. Remedy: Consumers should immediately turn off and unplug the recalled outdoor freezers and contact U-Line to schedule a free pickup of the recalled freezers and installation of a free replacement unit. Replacement options include a freezer, refrigerator drawers or refrigerator..

Details

Source

CPSC Consumer Product Recall

External ID

9417

Action Date

2022-10-13

Status

Recalled

Category

consumer_product

Product Description

This recall involves U-Line Outdoor Series 24-inch Built-In Convertible Freezers with model number U-1224FZRSOD-00A and

Context & Analysis

This is a unclassified recall.

This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

U-Line Corporation, of Milwaukee, Wisconsin 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 (U-Line Corporation, of Milwaukee, Wisconsin) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does U-Line Corporation, of Milwaukee, Wisconsin have FDA actions?

U-Line Corporation, of Milwaukee, Wisconsin 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 "9417" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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