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Coppertone is recalling five of its sunscreen products due to the presence of benzene, a chemical that can cause cancer with repeated exposure. Sunscreen recall 2021: Coppertone recalling select ...
The company that produces the popular sunscreen Banana Boat recalled three batches of spray bottles on Sunday over concerns they contained trace amounts of the cancerous chemical benzene. Edgewell ...
After Costco recalled several ready-to-eat chicken products earlier this month — including various Rana products — the discount giant has now added three new items to its growing recall list ...
The recalls came in response to reports of renal failure in pets consuming mostly wet pet foods made with wheat gluten from a single Chinese company, beginning in February 2007. The recall began voluntarily with the Canadian company Menu Foods on March 16, 2007, when a company test showed sickness and death in some of the test animals. Overall ...
Reported [31] cases of benzene contamination [32] have resulted in sunscreen recalls [33] initiated by regulators such as the TGA [34] and FDA or voluntarily by the brand. [35] Other reasons why the contamination likely occurred was the degradation of benzene-based (hydrocarbon) ingredients, [ 36 ] such as petrochemical UV filters [ 37 ] or ...
The original product dates to 1944, when pharmacist Benjamin Green invented a lotion to darken tans. [3] The product line has been expanded to include many skin care products, predominantly sunscreens. Coppertone has become the leading sun care brand in the United States, with annual $9 billion in global sales. [3]
The company behind Banana Boat is recalling more of its sunscreen products due to the presence of a cancer-causing chemical. Banana Boat expands sunscreen recall due to cancer risk Skip to main ...
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.