Super Herbs is voluntarily recalling all bottles of SUPER HERBS, light green and dark green capsules to the consumer level after FDA laboratory testing found SUPER HERBS to contain sibutramine, desmethylsibutramine, and/or phenolphthalein. … [Read more...]
Whole Foods Market Recalls Mislabeled Asparagus, Pea and Ricotta Salad Due to Undeclared Allergen
Whole Foods Market is recalling ten ounce packages of Asparagus, Pea and Ricotta salad because it was mislabeled and actually contained miniature Asparagus, Sun Dried Tomato and Swiss Frittatas. Due to the labeling error, an egg allergen was undeclared. … [Read more...]
Dexcom, Inc., Issues Press Release to Supplement Previous Customer Notification
Dexcom, Inc. (NASDAQ: DXCM) issues this press release to supplement its previous customer notification and remind its patients to periodically test the audible alarms and alerts on certain receivers manufactured by Dexcom to make sure that the audible alarms and alerts are functioning properly. The notification constituted a voluntary recall and … [Read more...]
Back to Nature Issues Allergy Alert for Limited Number of Classic Crème Cookies Due to Undeclared Milk
Back to Nature Foods, LLC is voluntarily recalling two (2) lots of its Classic Crème cookies, 12 oz packages, because it may contain undeclared milk, not listed as an ingredient on the label. Persons who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume this product. … [Read more...]
Voluntary Recall of Fetch™ 2 Aspiration Catheter
Boston Scientific (NYSE: BSX) has initiated a global, voluntary recall of all models of its Fetch™ 2 Aspiration Catheter, a thrombectomy catheter used during procedures to remove small blood clots from coronary arteries. The Fetch 2 catheters were recalled on March 22, 2016, due to complaints of shaft breakage. … [Read more...]
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