The blower’s shoulder straps, plastic buckles, or the anti-static ground wire can be drawn into the blower fan and fan housing causing plastic pieces to be expelled from the machine, posing laceration and impact hazards.
Source: Recall List
Vita Food Products, Inc. of Chicago, Illinois is notifying the public that it is recalling up to 8,376 individual plastic jars of 32 ounce Vita Wild Herring in Wine Sauce that are potentially mislabeled because they may contain sour cream and, therefor...
Source: FDA Food Safety Recalls RSS Feed
Hikma Pharmaceuticals PLC (Hikma, Group), today announces that its subsidiary Hikma Pharmaceuticals USA Inc. (formerly known as West-Ward Pharmaceuticals Corp.; “Hikma”) is voluntarily extending its previously-announced recall of certain lots (listed b...
Source: Food and Drugs Administration--Recalls/Safety Alerts
The recalled chest is unstable if it is not anchored to the wall, posing tip-over and entrapment hazards that may result in death or serious injuries to children. Additionally, KULLEN 3-drawer chests imported after August 12, 2019 do not comply w...
Source: Recall List
New Capstone, Inc. of Mooresville, NC is recalling their 22oz ReStructure Vanilla Protein Powder pouches, Lot 19211 Exp. 06/21 and their 27 gram individual serving pouch, Lot 19211 Exp. 06/21, because they may contain undeclared milk.
Source: FDA Food Safety Recalls RSS Feed
Whole Foods Market is voluntarily recalling select Green Chile Chicken Tamales from stores across 24 states because they contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening aller...
Source: Food and Drugs Administration--Recalls/Safety Alerts
Purina Animal Nutrition is initiating a voluntary recall of multiple lots of Purina® Rabbit Feed, Purina® Turkey Feed, Country Acres® Rabbit Feed and DuMOR® Chick Starter/Grower Feed due to elevated calcium levels in the product.
Source: Food and Drugs Administration--Recalls/Safety Alerts
American Health Packaging has voluntarily recalled eleven (11) lots of Ranitidine Tablets, USP 150 mg, 100 count Unit Dose Blisters to the consumer level due to the potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.
Source: Food and Drugs Administration--Recalls/Safety Alerts
The dining chairs can break, posing a fall hazard.
Source: Recall List
Internal electrical components can fail, allowing the units to overheat, posing a fire hazard.
Source: Recall List
