ISSUE: Bristol-Myers Squibb Company is voluntarily recalling one lot (#HN0063) of Eliquis 5 mg tablets to the consumer level. This lot was distributed nationwide in the U.S. to wholesalers and retail pharmacies in February 2017. Bristol-Myers Squibb is taking this precautionary measure based on a customer complaint that a bottle labeled as Eliquis 5 mg…

  Trouble starts when parents are in a hurry and forget to buckle up the kids and their friends before they take off in the family car. An accident occurs, children can be hurt and personal injury liability claims result from the friends’ parents. The National Highway Safety Administration reminds us that North Carolina’s “buckle…

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product: Product Description: The SpF® PLUS-Mini (60μA/W) & SpF® SpF XL IIB Implantable Spinal Fusion Stimulators Serial Numbers: SpF-XL IIB: 224595, 224598, 224607, 224608, 224610, 224613, 224615, 224621,…