SunTree Snack Foods, LLC. Issues Voluntary Recall of Dried Sweetened Strawberries Due to Potential Undeclared Sulfites

SunTree Snack Foods LLC, of Phoenix, AZ, is recalling Good & Gather Dried Sweetened Strawberries, because the product contains undeclared sulfite. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume these products

Source: Food and Drugs Administration--Recalls/Safety Alerts

Consumer Alert: Undeclared Sulfites in Dried “Wife Plum”

New York State Agriculture Commissioner Richard A. Ball today alerted consumers that A&C Best Food Trading Inc., located at 36-08 Review Ave in Long Island City, New York 11101, is recalling “Wife Plum” due to the presence of undeclared sulfites and unallowed dye E123. People who have severe sensiti

Source: Food and Drugs Administration--Recalls/Safety Alerts

Consumer Alert: Undeclared Sulfites in Dried “Wife Plum”

New York State Agriculture Commissioner Richard A. Ball today alerted consumers that A&C Best Food Trading Inc., located at 36-08 Review Ave in Long Island City, New York 11101, is recalling “Wife Plum” due to the presence of undeclared sulfites and unallowed dye E123. People who have severe sensiti

Source: Food and Drugs Administration--Recalls/Safety Alerts

Farm Fresh Produce LLC Recalls “TWA Agriculture Mixed Mushrooms” Because of Possible Health Risk

Farm Fresh Produce LLC of Vernon, CA, is recalling all of the 14.11 ounce packages of "TWA AGRICULTURE MIXED MUSHROOMS" because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elder

Source: Food and Drugs Administration--Recalls/Safety Alerts

Pfizer Voluntary Nationwide Recall of Lots of ACCURETICTM (Quinapril HCl/Hydrochlorothiazide), Quinapril and Hydrochlorothiazide Tablets, and Quinapril HCl/Hydrochlorothiazide Tablets Due to N-NitrosoQuinapril Content

Pfizer is voluntarily recalling Accuretic (quinapril HCl/hydrochlorothiazide) tablets distributed by Pfizer as well as two authorized generics distributed by Greenstone (quinapril and hydrochlorothiazide and quinapril HCl/ hydrochlorothiazide) to the patient(consumer/user) level due to the presence

Source: Food and Drugs Administration--Recalls/Safety Alerts

Pfizer Voluntary Nationwide Recall of Lots of Accuretic (Quinapril HCl/Hydrochlorothiazide), Quinapril and Hydrochlorothiazide Tablets, and Quinapril HCl/Hydrochlorothiazide Tablets Due to N-Nitroso-Quinapril Content

Pfizer is voluntarily recalling Accuretic (quinapril HCl/hydrochlorothiazide) tablets distributed by Pfizer as well as two authorized generics distributed by Greenstone (quinapril and hydrochlorothiazide and quinapril HCl/ hydrochlorothiazide) to the patient(consumer/user) level due to the presence

Source: Food and Drugs Administration--Recalls/Safety Alerts

Consumer Alert: Undeclared Sulfites in “Licorice Flavor Olive”

New York State Agriculture Commissioner Richard A. Ball today alerted consumers that A&C Best Food Trading Inc., located at 36-08 Review Ave in Long Island City, New York 11101, is recalling “Licorice Flavor Olive” due to the presence of undeclared sulfites. People who have severe sensitivity to sul

Source: Food and Drugs Administration--Recalls/Safety Alerts

Kao USA Conducts Expanded Voluntary Recall of Jergens® Ultra Healing Moisturizer

Select units of Jergens® Ultra Healing Moisturizer could show the presence of Pluralibacter gergoviae, a bacterium which typically poses little medical risk to healthy people. However, people who have certain health problems such as weakened immune systems may be more susceptible to infections. Kao

Source: Food and Drugs Administration--Recalls/Safety Alerts

Kao USA Conducts Expanded Voluntary Recall of Jergens® Ultra Healing Moisturizer

Select units of Jergens® Ultra Healing Moisturizer could show the presence of Pluralibacter gergoviae, a bacterium which typically poses little medical risk to healthy people. However, people who have certain health problems such as weakened immune systems may be more susceptible to infections. Kao

Source: Food and Drugs Administration--Recalls/Safety Alerts

Adamis Pharmaceuticals Corporation Issues Nationwide Voluntary Recall of SYMJEPI® (Epinephrine) Injection for Potential Manufacturing Defect

Adamis Pharmaceuticals Corporation (Nasdaq: ADMP) is voluntarily recalling certain lots of SYMJEPI (epinephrine) Injection 0.15 mg (0.15 mg/0.3 mL) and 0.3 mg (0.3 mg/0.3 mL) Pre-Filled Single-Dose Syringes to the consumer level. The batches in the table below are being recalled due to the potential

Source: Food and Drugs Administration--Recalls/Safety Alerts