Summitt Labs is voluntarily recalling Lot #730 Batch #K018 of KORE ORGANIC Watermelon CBD Oil Tincture, 30 ml bottle, 15mg 450x to the consumer level. The Florida Department of Agriculture and Consumer Services tested a random sample and found the prod...
Source: Food and Drugs Administration--Recalls/Safety Alerts
United Natural Foods, Inc. (UNFI) is initiating a voluntary recall of a limited quantity of Wild Harvest® Organic Basil distributed out of UNFI’s Hopkins, MN distribution center to select retailers in Minnesota between 4/18/2020-5/8/2020. UNFI’s recall...
Source: Food and Drugs Administration--Recalls/Safety Alerts
ICU Medical, Inc. is voluntarily recalling one single lot of Lactated Ringer's Injection, USP. The products are being recalled to the hospital/user level due to the presence of particulate matter identified as iron oxide. ICU Medical became aware of t...
Source: Food and Drugs Administration--Recalls/Safety Alerts
Zilk’s Plus Resources, LLC of Austin, TX announces a voluntary recall for select 12 oz bottles of Pluckers World Famous Wing Sauces because they may contain undeclared allergens.
Source: FDA Food Safety Recalls RSS Feed
Out of abundance of caution, and in line with its commitment to consumer satisfaction and safety, Becca Cosmetics is voluntarily recalling all shades of its Light Shifter Brightening Concealer because a brownish-black material identified as a common ho...
Source: Food and Drugs Administration--Recalls/Safety Alerts
The recalled magnet sets contain high-powered magnets and violate the federal standard for children’s toys. When two or more high-powered magnets are swallowed, they can link together inside a child’s intestines and clamp onto body tissues, causi...
Source: Recall List
The popcorn’s paper bag can catch fire in the microwave, posing fire and burn hazards.
Source: Recall List
The Reverse Fleece Hoodie fails to meet the federal flammability standards for clothing textiles, posing a risk of burn injuries to consumers.
Source: Recall List
MasterPharm, LLC. is voluntarily recalling 1 lot of Finasteride Plus 1.25mg, capsules to the consumer level. The Finasteride Plus capsules have been found to contain undeclared minoxidil, an antihypertensive drug, at levels greater than those found in ...
Source: Food and Drugs Administration--Recalls/Safety Alerts
The recalled chests are unstable and can tip over if not anchored to the wall, posing serious tip-over and entrapment hazards that can result in death or injuries to children.
Source: Recall List
