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Penumbra JET 7 Reperfusion Catheter with Xtra Flex Technology Recall

The Food and Drug Administration (FDA) has recently recalled all the configurations of the Penumbra JET 7 Xtra Flex due to the heightened risk of death or serio...

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Paragard IUD at the Heart of New Lawsuits 

Paragard is a copper intrauterine device, also known as an IUD, that many women use to act as a long-term birth control method. However, in recent years, this s...

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Possible Link Between Elmiron and Vision Loss

Elmiron, the brand name for pentosan polysulfate sodium (PPS), is a common prescription medication used to treat interstitial cystitis (IC) also known as painfu...

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Is Johnson & Johnson Targeting Minority Women to Sell Talc Powder?

An investigation into Johnson & Johnson’s talc-based baby powder products suggests the company may have targeted sales toward minority women. A recently r...

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DePuy Synthes Issues Elbow-Joint Replacement Recall

Several years ago, the medical device company DuPuy Synthes issued a recall of over 50,000 elbow-joint replacement devices. The device, referred to as a radial ...

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5 Year Anniversary Birmingham Hip Resurfacing (BHR) Recall

2020 marks the five-year anniversary of the recall for the Birmingham Hip Resurfacing (BHR) System manufactured by the medical device company, Smith and Nephew....

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The Link Between BIA-ALCL and Breast Implants

The Food and Drug Administration (FDA) has issued a press release regarding breast plant labeling and telling manufacturers to add a warning about the risk of b...

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Johnson & Johnson Sued For $2 Billion

Johnson & Johnson, a healthcare company that’s also the highest paid drug company in the world, is being charged for insurance fraud over opioids. Opi...

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Judge Sets Date for First 3M Earplug Bellwether Trial

A pretrial order was issued by United States District Judge Casey Rodgers on June 29, stating that the first 3M earplugs bellwether case would be going to trial...

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Drug Manufacturers Fail to Understand the Dangerousness of Zantac

At the end of last year the popular heartburn medication Zantac, or ranitidine, was recalled due to unsafe levels of N-nitrosodimethylamine (NDMA) found in it. ...

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