Ben’s Original is recalling a limited number of its rice products due to the possible presence of small stones, which pose a risk of oral or digestive tract injury if consumed, according to the U.S. Food and Drug Administration (FDA).
Black Sheep Eggs – Some of the recalled eggs, produced by the Black Sheep Egg Company of Arkansas, tested positive for seven strains of Salmonella, including several that can cause foodborne illness. – https://www.accessdata.fda.gov/scripts/ires/?Event=97655
Over 62,000 cans of sliced fruit have been recalled due to potential lead contamination, according to the Food and Drug Administration (FDA).1234
Pacific Coast Producers initially recalled the canned fruit cocktail and sliced pears—distributed by Wegmans and Walmart—on Sept. 4. On Oct. 10, the FDA gave the recall the second-highest risk level. Read More –
FDA Expands Massive Pasta Recall Linked to 4 Deaths and 19 Hospitalizations
Pet Parents Urged to Check Freezers After FDA Announces Recall – Yahoo Yahoo The FDA confirmed that Raw Bistro Pet Fare has voluntarily recalled its Frozen Beef Entrée for Dogs after routine testing detected potential …
The FDA Has Issued an Urgent Nationwide Recall for a Popular Frozen Vegetable – El Diario 24 El Diario 24
Over the past few months, the Food and Drug Administration (FDA) has made several recalls of certain products. The recalls are continuously …
FSIS Issues Public Health Alert For Ready-To-Eat Meals Containing Spinach That May Be Contaminated With Listeria
FSIS Issues Public Health Alert For Ready-To-Eat Meals Containing Spinach That May Be Contaminated With Listeria The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for FSIS-inspected ready-to-eat meals produced by FreshRealm containing a Food and Drug Administration (FDA) regulated ingredient, specifically spinach, that may be contaminated with Listeria monocytogenes (Lm).
FDA announces recall for Johnson & Johnson devices due to cybersecurity risk—customers … Cardiovascular Business The FDA and Johnson & Johnson MedTech are telling customers to keep the devices in a secure environment until they can be disabled from all …
FDA details Class I recalls for more than 1 million pacemakers—software update required Cardiovascular Business The FDA has finalized new Class I recalls related to ongoing safety concerns with Boston Scientific’s Accolade family of pacemakers.
Most serious FDA recall issued for Abiomed heart pump controllers | AHA News
FDA Drug Recalls and Warnings: Illegal GLP-1 Sales and Misleading Marketing by Novo …