The products contain potassium hydroxide and sodium hydroxide which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of chemical burns a...
Source: Recall List
The bolt on the electric scooter can come loose causing the suspension and wheel assembly to separate, posing fall and injury hazards.
Source: Recall List
The recalled glass doorknobs can crack and separate from the doorknob assembly, posing a laceration hazard to consumers.
Source: Recall List
The bolts used to secure the seat of the recalled highchair to the pedestal base can become loose and allow the seat to detach, posing a fall hazard.
Source: Recall List
The main injector fuel return hose can leak, posing a fire hazard. This can also result in serious property damage, injuries or even death.
Source: Recall List
TODORGANIC INC Middleburg FL está retirando del mercado sus semillas Nuez de la India porque un análisis de la FDA ha determinado que las semillas parecen ser Thevetia peruviana o adelfa amarilla. Se sabe que todas las partes de la planta de adelfa ama...
Source: Food and Drugs Administration--Recalls/Safety Alerts
TODORGANIC INC Middleburg FL is recalling its Nuez de la India Seeds because FDA analysis has determined that the seeds appear to be Thevetia peruviana, or yellow oleander. All parts of the yellow oleander plant are known to contain cardiac glycosides ...
Source: Food and Drugs Administration--Recalls/Safety Alerts
The Ice Cream House is voluntarily recalling all Dairy Ice Cream Products and Non-dairy [Parve] frozen Dessert products due to potential health risk in regards to Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and s...
Source: Food and Drugs Administration--Recalls/Safety Alerts
New Castle, Delaware, Marlex Pharmaceuticals, Inc. is voluntarily recalling one lot of Digoxin Tablets USP, 0.125mg and one lot of Digoxin Tablets USP, 0.25mg to the consumer level due to Label Mix-Up. Bottles of Digoxin Tablets, USP 0.125mg s are inco...
Source: Food and Drugs Administration--Recalls/Safety Alerts
On July 1, 2023, Universal Meditech Inc. initiated a nationwide recall of products it manufactured between March 2021 and November 2022. The recall is due to the reasons that: i.The company is going out of business, hence would not be able to continue ...
Source: Food and Drugs Administration--Recalls/Safety Alerts
