Neptune Resources, LLC is voluntarily recalling All lots of Neptune's Fix Elixir, Neptune's Fix Extra Strength Elixir, and Neptune's Fix Tablets to the consumer level. Neptune Resources LLC's distribution channels have not reported any adverse events from the use of its products. The products are be
Source: Food and Drugs Administration--Recalls/Safety Alerts
Navigating child labor laws and the general workforce as an underage worker can be a challenging experience. It’s essential to be aware of the legal protections in place at both the federal and state levels. In this blog post, we will explore the rights of underage workers under federal law and specific protections provided by […]
Utz Quality Foods, LLC., is issuing a voluntary recall for 88 cases of Utz® 2.75 oz. Wavy Original Potato Chips due to an undeclared milk allergen. This recall was initiated after Utz learned that approximately 1200 single-serve bags contained Utz® Wav...
Source: FDA Food Safety Recalls RSS Feed
The portable fuel bottles do not meet the child-resistant requirements for closures under the Children's Gasoline Burn Prevention Act (CGBPA). The closure for the products is not child-resistant, posing a risk of burn and poisoning to children.
Source: Recall List
The wiring harness that manages the charging of the lithium-ion battery was not properly assembled, creating a risk of overheating and fire while charging.
Source: Recall List
The rhinestones embedded in the recalled tiaras contain levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health effects.
Source: Recall List
The fan’s blade can crack or break and fall off the unit, posing an impact injury hazard.
Source: Recall List
The plastic chairs can break apart while in use, posing a fall hazard.
Source: Recall List
Woburn, Massachusetts, Azurity Pharmaceuticals, Inc. is voluntarily recalling one (1) lot (F230169A) of Zenzedi® CII (dextroamphetamine sulfate tablets, USP) 30 mg to the consumer level. The product is being recalled due to a report from a pharmacist i...
Source: Food and Drugs Administration--Recalls/Safety Alerts
Woburn, Massachusetts, Azurity Pharmaceuticals, Inc. is voluntarily recalling one (1) lot (F230169A) of Zenzedi® CII (dextroamphetamine sulfate tablets, USP) 30 mg to the consumer level. The product is being recalled due to a report from a pharmacist i...
Source: Food and Drugs Administration--Recalls/Safety Alerts
