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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.
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 ...
The Certified USB Fast Charger logo indicating support for the Programmable Power Supply (PPS) protocol in USB Power Delivery (PD) chargers On January 8, 2018, USB-IF announced the Certified USB Fast Charger logo for chargers that use the Programmable Power Supply (PPS) protocol from the USB Power Delivery 3.0 specification.
Eye drops are being recalled due to a rare bacterium found in artificial tears. Find a list of recalled drops in 2023. Plus, eye infection symptoms.
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A product recall is a request from a manufacturer to return a product after the discovery of safety issues or product defects that might endanger the consumer or put the maker or seller at risk of legal action. Product recalls are one of a number of corrective actions that can be taken for products that are deemed to be unsafe.
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