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Gourmet Snack Line Recalled for Undeclared Allergies

Snacks On Racks Inc. is recalling dozens of products from its retail locations due to the lack of adequate warnings for a number of potential food allergens. These products are only sold in food service establishments throughout the continental United States, and all bear a blue Snacks on Racks label. They are not sold at […]


Recall Issued for Undeclared Allergies on Fish Product

Superior Foods Company of Grand Rapids Michigan issued a recall for its Lemon Pepper Marinated Catfish and Cajun Style Catfish because of missing information on potential allergens. The lemon pepper catfish contains undeclared soy and FD&C Yellow #5 (also known as Tartrazine). The Cajun catfish has undeclared soy products. The presence of these products may […]


Vita Food Products Recalls Herring Dish for Improper Labeling

A Chicago food company, Vita Food Products, has issued a voluntary recall on November 24 of its Elf Branded Herring in Sour Cream product for failure to disclose the presents of wheat in the ingredients. The failure to disclose this ingredient may put people who suffer from wheat allergies, or who are following a gluten […]


Cardiovascular Systems Initiates Recall of Defective Catheter Introducer

On November 16, 2009, Cardiovascular Systems announced a recall of all lots of its ViperSheath catheter sheath introducer based on reports of stretching or fracturing of the product. The ViperSheath is a coil-reinforced catheter introducer of percutaneous entry of intravascular devices. If a fracture occurs, there is a potential for a segment to break off […]


Stryker Issues a Class I Recall of Surgical Navigation Systems

Stryker Corporation, a leading medical technology company, is recalling 23 of its navigation systems because of a potential issue for a component to stop working. The failure may cause the navigation screen to freeze, a delay in system updates, or failure to respond to input. These types of delays can have devastating effects in the […]


Automated External Defibrillators Subject to Voluntary Field Correction

Cardiac Science, makers of several types of automated external defibrillators, AED, issued a call for a field correction of some of its devices. A problem was discovered that might hinder a resuscitation event, which could lead to severe medical issues including death. The affected models include: CardioVive 92531, 92532, and 92533 devices Powerheart 9300A, 9300C, […]


Allergy Alert on Toi Sauce Thai Red Curry Issued by Redmond Washington Company

Rikki USA, Inc. is re-issuing a recall on its Toi Sauce Thai Red Curry (Panang) for undeclared shrimp in one of the sub ingredients. According to the company, a label made by an outsourced company, SIAMRICA Co, failed to warn of shrimp ingredients in the red curry paste. People with severe allergies to shrimp may […]


Large Seedless Watermelons Recalled for Salmonella Contamination

Timco Worldwide Inc. is recalling “MelonUp” large seedless watermelons that were distributed to select grocers, wholesalers, and processors in Texas and California. Salmonella bacteria were discovered during the course of routine testing of a randomly selected melon. No illnesses have yet been reported in connection with this product. The recall involves large seedless watermelons labeled […]


Mislabeled Margarine Leads to ConAgra Recall

ConAgra foods notified the FDA on November 13 about a report of mislabeled tubs of Blue Bonnet Spread. The tubs and lids indicated that the product was Blue Bonnet Light Spread, when in reality; it was regular Blue Bonnet Spread. This poses a problem because the ingredients do not list milk (whey), which is a […]


Class I Recall of Vertebral Replacement by Synthes USA

The FDA and Synthes USA have declared a class I recall of the Ti Synex II Vertebral Body Replacement (VBR) product. This device is used to replace damaged T1 – L5 vertebral material during replacement surgery. The FDA received six adverse event reports that lead to the recall. The reports indicated a failure of the […]

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