Felt, OK, McDaniel Life-Line LLC is voluntarily recalling all lots of Indian Herb to the consumer level. This product is being recalled because it is marketed without an approved NDA/ANDA. The therapeutic claims made in the labeling for this product establish that it is a drug because it is an article (other than food) intended to affect the structure or any function of the body. Additionally, the product contains ingredients that the Agency has determined to be caustic in nature that can cause serious injury. (US Food Recalls) More
Felt, OK, McDaniel Life-Line LLC is voluntarily recalling all lots of Indian Herb to the consumer level. This product is being recalled because it is marketed ...
Posted on 8 February 2019 | 6:41 pm | Google News
Tesla will cut 7 percent of its workforce as it tries to lower prices and break out of the niche-car market to produce an electric vehicle that more people can afford.
Posted on 18 January 2019 | 3:00 am | Google News
NEW YORK (AP) - President Donald Trump's estranged former lawyer is acknowledging that he paid a technology company to rig Trump's standing in two online ...
Posted on 17 January 2019 | 3:00 am | Google News
Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API) US Recall News
Sandoz Inc. is voluntarily recalling one lot of Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25mg to the consumer level. This product is being ...
Posted on 9 November 2018 | 3:00 am | Google News
Urgent: Curry Spice Recall US Recall News
This is to inform you of a product recall involving: HOT CURRY POWER & CURRY POWDER, BARAKA, 7.0 oz PLASTIC JAR UPC CODES 822514265566 AND ...
Posted on 25 October 2018 | 2:00 am | Google News