Search results
Results from the WOW.Com Content Network
Coldspot was a brand by US retail company Sears that existed from 1928 to 1976, when it was replaced with the Kenmore brand. [1] The brand was originally created for a line of refrigerators. Other products sold under the Coldspot brand included freezers, dehumidifiers, and window air conditioning units.
Bad news for people hoping to use their pricey, recently purchased ranges to roast turkeys or bake pies for Thanksgiving. High-end ranges sold under the Kenmore and Electrolux brands are being ...
Various Kenmore kitchen stoves and other appliances at a Sears Outlet store. Kenmore's upscale line of products is known as the Elite line. Kenmore also has a professional line of appliances called Kenmore Pro. As of January 2019, the Kenmore brand had over 50 products listed as top performers on the non-profit website Consumer Reports. [16]
Product recalls are one of a number of corrective actions that can be taken for products that are deemed to be unsafe. The recall is an effort to limit ruination of the corporate image and limit liability for corporate negligence, which can cause significant legal costs. It can be difficult, if not impossible, to determine how costly can be ...
The recalled dehumidifiers can be identified by their brand, model number and capacity, which is all listed on the CPSC's notice. The products are white, beige, gray or black plastic — sold in ...
The recall involves slide-in electric ranges with front-mounted knobs that can be turned on accidentally by people or pets, ... Recalled model numbers: NE58K9430SS/AA NE58N9430SG/AA NE58R9431SG/AA ...
Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.