Avas 8 oz. Organic Roasted Unsalted Almonds UPC 8-10111-01032-0
Severn Peanut Co., Inc.
Product may be contaminated with Listeria monocytogenes.
92,900 total recalls in our database
Severn Peanut Co., Inc.
Product may be contaminated with Listeria monocytogenes.
Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments.
Product contaminated with Listeria monocytogenes
Severn Peanut Co., Inc.
Product may be contaminated with Listeria monocytogenes.
ProSupps USA
Product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
ProSupps USA
Product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
Product contaminated with Listeria monocytogenes
International Flavors & Fragrances
Seasoning blends may contain salmonella.
The firm was notified that the product does not list MILK in the allergen Contains statement, although it is listed in the ingredient statement. They were alerted of this error by a consumer who reported a reaction consistent with a Milk allergy.
ProSupps USA
Product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
Failed Impurities/Degradation Specifications: stability testing results did not meet the specification for impurities.
Apothecary By Design
Lack of Processing Controls: The metal container closure adheres to the rubber stopper on some of the units of the batch which can impact the integrity of the container closure.
Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the batch contains Day-Night Cough Liquid.
Superpotent Drug: high out-of-specification result for magnesium.
Mckesson Packaging Services
Failed Moisture Limits: Product tested out-of-specification for moisture content.
Noven Pharmaceuticals
Defective Delivery System: Out of specification for peel force from the release liner specification during stability testing at 18M 25C/60%RH.
Labeling: Not Elsewhere Classified. Manufacturer and product were discovered to be on FDA Import Alert 66-66 for misbranding of active pharmaceutical ingredient.
The device collar size was incorrectly labeled as 25 mm where it should be recorded as 32 mm
Under certain conditions, the cables used with the Hemo system during a patient procedure could stop displaying the patient SpO2 causing a slight delay in patient care.
ROTH MOBELI grab handles could detach and patient could fall if the EOS system operator does not follow instructions. Before each use, the operator must examine the vacuum safety indicator to check the vacuum is monitored and sufficient and the grab handle correctly attached. Do not use grab handles to help patient up. The handles are only for stabilizing the patients hand or arm in the EOS cabin.