View post: Aura Nismo RS Debuts as the Toyota GR Yaris Fighter Nissan Wants to Build Ford recalls 272,645 vehicles due to rollaway risk from faulty park module software. F-150 Lightning, Mustang ...

Ford issued a recall for more than 272,000 hybrid and electric vehicles due to a software glitch that could cause them to roll away on their own. Which EVs and hybrids are included in Ford’s recall?

Mary Cunningham is a reporter for CBS MoneyWatch. She previously worked at "60 Minutes," CBSNews.com and CBS News 24/7 as part of the CBS News Associate Program. Ford Motor is recalling nearly 273,000 ...

Ford is recalling more than 272,600 examples of its vehicles over an issue with the integrated park module, which may lead to vehicles rolling away. Related: More Ford News Affected vehicles include ...

SPOKANE, Wash. -- The U.S. Attorney's Office says an eastern Washington doctor pled guilty to augmenting recalled medical devices to sell them as new to patients. According to the U.S. Attorney's ...

Megan Cerullo is a New York-based reporter for CBS MoneyWatch covering small business, workplace, health care, consumer spending and personal finance topics. She regularly appears on CBS News 24/7 to ...

This story was originally published by ProPublica. The FDA rarely uses its authority to pull dangerous medical devices off the market and is so poorly staffed that it's sometimes unable to make sure ...

Dec 16 (Reuters) - Ford Motor (F.N), opens new tab is recalling 32,160 vehicles in the United States, as loss of drive power increases the risk of a crash, the U.S. National Highway Traffic Safety ...

This story was originally published by ProPublica. Sign up for The Big Story newsletter to receive stories like this one in your inbox. The Food and Drug Administration rarely uses its authority to ...

The U.S. National Highway Traffic Safety Administration on Monday opened a probe into the recall of 331,401 Jeep vehicles due to improperly installed rear coil springs. A rear coil spring helps the ...

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This article originally appeared on ProPublica. The Food and Drug Administration rarely uses its authority to pull dangerous medical devices off the market and is so poorly staffed that it’s sometimes ...