Wayne Hogan

Practice Areas: Defective Products

Toyota Recalls Prius Hybrids

Toyota has recalled 106,000 first-generation Prius hybrid cars globally for faulty steering caused by a nut that may come loose. The single minor accident suspected of being related to the problem was reported in the United States, according to Toyota Motor Corp. The latest recall from Toyota affects 48,000 Prius vehicles in Japan, starting with […]

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12/14/10 – Rolaids Recall – Foreign Materials in Products

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc. recalled all lots of Rolaids Extra Strength Softchews, Rolaids Extra Strength plus Gas Softchews, and Rolaids Multi-Symptom plus Anti-Gas Softchews distributed in the United States, following consumer reports of foreign materials in the product, including metal and wood particles. Rolaids Extra Strength Softchews, Rolaids Extra Strength plus Gas […]

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7/14/2010 Pottery Barn Kids Recalls to Repair Drop-Side Cribs Due to Entrapment, Suffocation and Fall Hazards

CPSC Recall Hotline: (800) 638-2772 WASHINGTON, D.C. – The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product. Name […]

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Thoratec Corporation Issues Worldwide Medical Device Correction of HeartMate II

Recall — Firm Press Release FDA posts press releases and other notices of recalls and mar Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product […]

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FDA Warns Consumers Against Using Mommy’s Bliss Nipple Cream

FOR IMMEDIATE RELEASE May 23, 2008 FDA Warns Consumers Against Using Mommy’s Bliss FOR IMMEDIATE RELEASE May 23, 2008 FDA Warns Consumers Against Using Mommy’s Bliss Nipple Cream Product can be harmful to nursing infants The U.S. Food and Drug Administration is warning consumers not to use or purchase Mommy’s Bliss Nipple Cream, marketed by […]

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02/17/08 Fentanyl Patches Recalled

More Fentanyl Patches Recalled Actavis Recalls Certain Fentanyl Patches in the US as Precaution Media Contact: Actavis Inc. Sarita Thapar, PharmD 908-659-2471 FOR IMMEDIATE RELEASE — Morristown, NJ — February 17, 2008 — Actavis Inc., the United States manufacturing and marketing division of the international generic pharmaceutical company Actavis Group hf, today announced that 14 […]

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02/12/08 Johnson & Johnson Duragesic Fentanyl Patches

Johnson & Johnson Unit Recalls 25 Mcg/Hr Duragesic Patches February 12, 2008: 03:32 PM EST Johnson & Johnson’s PriCara unit recalled all lots of 25-microgram-per- hour Duragesic CII pain patches that may have a cut edge that could leak fentanyl gel. The recalled patches, manufactured by Alza Corp. and sold by PriCara and Sandoz Inc. […]

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VIOXX:Trials for Pioneering Terrell Hogan Client

In May 2001 Evelyn Plunkett’s husband, Dickie, died of a sudden heart attack after taking VIOXX. Evelyn suspected the drug, made by Merck, caused her husband’s death. She engaged Terrell Hogan to investigate and pursue her claim to get to the bottom of the VIOXX story: what Merck knew, and when it knew it. Now, […]

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FAQ’s Concerning the Medtronic Sprint Fidelis Recall

1. What is a defibrillator lead? Leads are thin insulated wires connected to a defibrillator that carry electric impulses to the heart in patients with a heart rhythm abnormality. 2. Why has Medtronic recalled its Sprint Fidelis defibrillator leads? Medtronic actually refuses to call its actions a recall.

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