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      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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      Dated: MAY 16, 2022 Daimler Trucks North America, LLC (DTNA) is recalling certain 2021-2022 FCCC MT50e walk-in vans. The rotary shift position knob … [Read More...]

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You are here: Home / Search for "dietary supplement"

Search Results for: dietary supplement

Genetic Edge Compounds Issues Voluntary Nationwide Recall of GEC Laxoplex Dietary Supplement Capsules Due to Presence of Anabolic Steroids

May 5, 2017 By The FDA Leave a Comment

Genetic Edge Compounds is voluntarily recalling all lot codes distributed between February 2, 2015- May 2, 2017 of GEC Laxoplex dietary supplement capsules, packaged in a white plastic bottle containing 60 capsules to the retail level and consumer level. Food and Drug Administration (“FDA”) analysis has found GEC Laxoplex to be tainted … [Read more...]

Filed Under: FDA Press Releases

A&H Focal Inc. Issues Nationwide Recall of 29 Products Marketed as Dietary Supplements Due to The Possible Presence of Undeclared Erectile Dysfunction Ingredients

March 8, 2017 By US Recall News Leave a Comment

A&H Focal Inc. is voluntarily recalling all lots of the following products because many of these products have been historically tested by the FDA and found to contain PDE-5 Inhibitors (i.e. sildenafil, tadalafil, vardenafil, etc.) which is the active ingredient in an FDA-approved drug for erectile dysfunction (ED) making these tainted dietary … [Read more...]

Filed Under: FDA Press Releases

Kingsway Trading Inc. Recalls “Xanthium & Siler Combo (Bi Yan Pian) Dietary Supplement” because it Contains Banned Ephedra Alkaloids

February 8, 2017 By The FDA Leave a Comment

Kingsway Trading Inc. of Brooklyn, NY is recalling its 1.06 oz (30g) bottles of “Well Balance Xanthium & Siler Combo (Bi Yan Pian)” Batch No. 130401 & Batch No. 150201 because they contain the presence of undeclared Ephedra Herba (ma huang), an FDA banned item. Dietary supplements containing ephedrine alkaloids pose a risk of serious … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

MS Bionic, Inc. Issues a Voluntary Nationwide Recall of All Lots of Megajex Natural Male Sex Enhancer Dietary Supplement

November 30, 2016 By The FDA Leave a Comment

MS Bionic, Inc. announced today that it is conducting a voluntary nationwide recall of all lots of Megajex Natural Male Sex Enhancer capsules. FDA analysis has found the product to contain Tadalafil and Sildenafil. … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Nutra Manufacturing, Inc. Announces Nationwide Voluntary Recall of One Lot of GNC Women’s Ultra Mega Time Release 180 count Dietary Supplement

November 18, 2016 By The FDA Leave a Comment

Pittsburgh, PA, Nutra Manufacturing, Inc. (“Nutra”) today announced that it is initiating a nationwide, voluntary recall of one lot of GNC Women’s Ultra Mega Time Release dietary supplement product sold in 180 count containers UPC 048107158910, lot number 3044FQ2024, with an expiration date of June 2018 due to the fact the product may contain an … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

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J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

FCCC ( 22V340000 )

May 20, 2022 By NHTSA

FREIGHTLINER ( 22V339000 )

May 20, 2022 By NHTSA

RICH SPECIALITY TRAILERS ( 22V336000 )

May 20, 2022 By NHTSA

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J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

FORD ( 22V333000 )

May 19, 2022 By NHTSA

LINCOLN ( 22V346000 )

May 19, 2022 By NHTSA

White Cane Sockeye Salmon LLC Issues Allergy Alert on Undeclared Wheat and Soy in Wild Alaskan Cooked and Smoked Salmon

May 18, 2022 By The FDA

QueensMade Lemonade Issues a Voluntary Recall Due to Products Being Adulterated

May 18, 2022 By The FDA

Moderne Glass Company Recalls Coffee Cups Due to Burn Hazard (Recall Alert)

May 18, 2022 By The CPSC

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

QueensMade Lemonade Issues a Voluntary Recall Due to Products Being Adulterated

May 18, 2022 By The FDA

Moderne Glass Company Recalls Coffee Cups Due to Burn Hazard (Recall Alert)

May 18, 2022 By The CPSC

DGL Group Recalls Hover-1 Superfly Hoverboards Due to Fall and Injury Hazards

May 18, 2022 By The CPSC

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