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Food & drugs

Megajex Natural Male Sex Enhancer by MS Bionic: Recall - Undeclared Drug Ingredients

01-12-2016

Undeclared tadalafil and sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels.

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Ultimate Body Tox PRO: Recall - Undeclared Drug Ingredient

01-12-2016

Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke.

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Ultimate Body-Tox Issues a Nationwide Voluntary Recall of Ultimate Body Tox PRO Found to Contain Undeclared Sibutramine

01-12-2016

High Point, NC, Ultimate Body-Tox is voluntarily recalling all lots of Ultimate Body Tox PRO capsules to the consumer level. FDA analyses of this product found it to contain undeclared sibutramine. Sibutramine is a controlled substance that was...

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

30-11-2016

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.

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Calbee North America Issues Allergy Alert On Undeclared Milk In Harvest Snap Black Pepper Snap Pea Crisps

28-11-2016

Calbee of Boardman, Oregon is recalling 3,588 cases of Harvest Snap Black Pepper snap pea crisps are in 3.3 oz bags and have Lot Number MAR 31 17 0141 S. Harvest Snap Black Pepper snap pea crisps may actually contain Harvest Snap Wasabi Ranch snap...

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DMAA Net Weight 500g by NutriVitaShop: Recall - Presence of DMAA May Pose Health Risk

26-11-2016

DMAA can narrow blood vessels and arteries, which can cause a rise in blood pressure or other cardiovascular problems such as shortness of breath, arrhythmias, tightening in the chest, and heart attack.

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JFC International Inc. Issues Allergy Alert On Undeclared Wheat In You-Ka Fresh Ramune And You-Ka Punch Ramune

25-11-2016

Los Angeles, CA - JFC International Inc. is voluntarily recalling the following confectionery products because they may contain undeclared wheat. People who have allergies to wheat run the risk of a serious or life-threatening allergic reaction if...

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Anderson’s Frozen Custard issues Allergy Alert on Undeclared Peanuts in Pumpkin Ice Cream Pies

25-11-2016

Anderson’s Frozen Custard is recalling its “Pumpkin Ice Cream Pies” Because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life threatening allergic reaction if they consume these products.

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Products Containing Belladonna Extract by Raritan Pharmaceuticals: Recall - Possible Belladonna Alkaloids

25-11-2016

The homeopathic products have a very small amount of belladonna, a substance that can cause harm at larger doses.

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Product Label Missing Milk and Fish Allergen Advisory in Blue Crab Mini Crab Cakes

24-11-2016

Salisbury, Maryland - Handy Seafood Incorporated (“Handy”) is voluntarily recalling approximately 71 cases of Blue Crab Mini Crab Cakes, as identified on Attachment A. The voluntary recall is limited to this product which was distributed to...

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Raritan Pharmaceuticals Inc. Issues a Voluntary Nationwide Recall of Products Containing Belladonna Extract Due to the Possibil

24-11-2016

Raritan Pharmaceuticals, a contract manufacturer for Homeolab USA, is voluntarily recalling homeopathic products containing belladonna extract (see products below) due to the potential for variation in the content of belladonna extract in the...

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Nutrivitashop, A DBA of Naturecom Inc is Requesting the Voluntarily Recall of DMAA Net Weight 500g Due to the Presence of DMAA

24-11-2016

NutriVitaShop is a dba of Naturecom Inc. Lake Forest, CA is requesting the voluntary nationwide recall of its DMAA net weight 500g to include lot #20141102, 20150715, 20151022, 20160226, 20160701, 20161017 and 20150323 because there may be presence...

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This update to the February 2020 safety communication provides information on the final guidance, Product Labeling for Laparoscopic Power...

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