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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.
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.
Vita Green Health Products Co., Ltd. (Chinese: 維特健靈), also as known as Vita Green, is a manufacturer and distributor of health and beauty products in Hong Kong. The company was set up in 1993 with two GMP certified factories. [2] Vita Green has developed from its Hong Kong base and now has offices in Asia, Europe and United States. [1]
Listeria caused a recall of cucumbers sold at Walmart stores in three states, but that recall has mushroomed into a recall of cucumbers, green beans, cilantro and peppers from Walmart, Aldi ...
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Health. Health. Fitness. Medicare. Main Menu. News. News. Entertainment. Lighter Side. Politics. ... Below is a list of specific carrot lots affected by the recall. Whole carrot brands and ...
Unilever voluntarily recalled two types of Suave spray deodorant on March 30 after they were found to contain “slightly elevated levels” of a cancer-causing ingredient called benzene ...
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 ...