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      J&J Settles Talc Mesothelioma Settlement

      By Sandra Dalton, Staff Writer On January 6, 2020, Superior Court Judge Stephen Kaus announced that Johnson & Johnsons (J&J) had agreed to … [Read More...]

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      The ramps cannot withstand the weight of equipment within the limits that are specified on the ramps and can bend or break while in use, posing a fall … [Read More...]

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You are here: Home / Archives for Food Recalls / FDA Press Releases

The Medicines Company Recalls Certain Lots of Cleviprex: Particulate Matter

December 17, 2009 By The FDA Leave a Comment

The Medicines Company (NASDAQ: MDCO) announced today that it is voluntarily recalling eleven (11) lots of Cleviprex ® (clevidipine butyrate) injectable emulsion due to the potential presence of visible particulate matter which has been observed in some vials during a routine annual inspection. The affected Cleviprex lots are 61-978-DW, 61-979-DW, … [Read more...]

Filed Under: FDA Press Releases

Atlas Operations Recalls Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements

December 15, 2009 By The FDA 2 Comments

Pompano Beach, FL – Atlas Operations, Inc. announced today that it is conducting a voluntary nationwide recall of the company's dietary supplements for sexual enhancement sold under Lot Numbers 494, 520C, 520B, 520A, 520, 521, 705, 706, 779 & 807. These products are currently being sold as a dietary supplement throughout the U.S. Atlas Operations, … [Read more...]

Filed Under: FDA Press Releases

Stryker Operating Room System II Surgical Navigation System – Recall

December 11, 2009 By The FDA Leave a Comment

Recall Class: Class I Date Recall Initiated:  October 26, 2009 Product:  Operating Room System II Surgical Navigation Systems Product Name Stryker Catalog Number Serial#/Lot# Range Navigation System II-Cart 7700-100-000 Serial #s 100715-100735 PC SPC-1 Assembly 7700-101-201 Lot # K7P00F6000 These devices were manufactured … [Read more...]

Filed Under: FDA Press Releases

Bayer Recalls One Lot of Alka-Seltzer Plus Day & Night Cold Formula Liquid Gel Combo Packs

December 9, 2009 By The FDA Leave a Comment

In consultation with the U.S. Food and Drug Administration (FDA), Bayer’s Consumer Care division has begun a voluntary recall of a single product lot of the combination package of Alka-Seltzer Plus® Day & Night Cold Formula Liquid Gels. Bayer initiated the recall after identifying that the labeling on the foil blister card of certain packages … [Read more...]

Filed Under: FDA Press Releases

Cardiovascular Systems ViperSheath Sheath Introducer – Recall

December 5, 2009 By The FDA Leave a Comment

Recall Class: Class I Date Recall Initiated: October 21, 2009 Product: ViperSheath Sheath Introducer is manufactured by Thomas Medical Products, Inc. and is distributed by Cardiovascular Systems, Inc. (CSI). Lot Ranges Catalog Numbers S28117 through S29174 VPR-ISH 5 X 85, VPR-ISH 6 X 85, VPR-ISH 7 X 85, VPR-ISH 5 X 45, VPR-ISH 6 X 45, VPR-ISH 7 … [Read more...]

Filed Under: FDA Press Releases

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Economic Consulting

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Tractor Supply Recalls Traveller Aluminum Loading Ramps Due to Fall Hazard

July 16, 2025 By The CPSC

Deale International Recalls CasaClean Handheld Steamers Due to Risk of Serious Burn Injury; Sold on HSN

July 16, 2025 By The CPSC

iStore Magnetic Wireless Power Banks Recalled Due to Fire and Burn Hazards; Imported by Tomauri

July 16, 2025 By The CPSC

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

VIVI E-Bikes Lithium-ion Batteries Sold with VIVI E-Bikes Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Sold by VIVI

July 16, 2025 By The CPSC

Chetak LLC Group Recalls Product Because of Possible Health Risk

July 16, 2025 By The FDA

Krasniy Oktyabr Inc. USA Issues Alert on Eviscerate Dry Salted Vobla “Aral Silver”

July 15, 2025 By The FDA

BD Issues Update to Voluntary Global Recall of Alaris™ and BD Alaris™ Pump Modules Serviced with Legacy Bezel Kit Assemblies

July 15, 2025 By The FDA

World Market Recalls Emek Spread Pistachio Cacao Cream with Kadayif Due to Salmonella Contamination

July 14, 2025 By The FDA

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

BD Issues Update to Voluntary Global Recall of Alaris™ and BD Alaris™ Pump Modules Serviced with Legacy Bezel Kit Assemblies

July 15, 2025 By The FDA

World Market Recalls Emek Spread Pistachio Cacao Cream with Kadayif Due to Salmonella Contamination

July 14, 2025 By The FDA

YoCrunch® Products Voluntarily Recalled by Danone U.S. Due to Potential Presence of Plastic Pieces in Dome Topper

July 14, 2025 By The FDA

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-- See More Recall News

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