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Consumers should immediately stop using the recalled portable chargers and contact myCharge at 888-251-2026 or compliance@mycharge.com for a free replacement portable charger, the company said. ...
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.
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 ...
Old logo (1972-2018) The United States Consumer Product Safety Commission (USCPSC, CPSC, or commission) is an independent agency of the United States government.The CPSC seeks to promote the safety of consumer products by addressing "unreasonable risks" of injury (through coordinating recalls, evaluating products that are the subject of consumer complaints or industry reports, etc ...
Nokia is recalling an estimated 14 million cell phone chargers the company says might be defective and could cause users to get shocked. The Finnish mobile telecommunications giant said it found ...
This recall covers five scents and sizes from 22 ounces to 1 gallon. There was a similar recall last year of Pine-Sol. 4.9 million bottles of Fabuloso recalled for a potential bacterial contamination
The 2014 and 2015 versions of Pump Express, Pump Express Plus and Pump Express Plus 2.0, differ from by communicating voltage requests to the charger using current modulation signals through the main USB power lanes (VBUS) rather than negotiating through the USB 2.0 data lanes.
In 2013, MedWatch introduced Form 3500B, which is designed to facilitate reporting by healthcare consumers. [4] The MedWatch system is intended to detect safety hazard signals for medical products. If a signal is detected, the FDA can issue medical product safety alerts or order product recalls, withdrawals, or labeling changes to protect the ...