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Product is sub-potent for Vitamin D and label contains incorrect percent daily value.
Misprint on tablet
Label error during reprint. Says 1000 mg instead of 1000 mcg on the center front panel of the label.
Amount of Phosphatidyl Serine in product is less than stated on the label
Undeclared milk
Superpotent drug: Assay results were slightly above specification at the time zero point.
Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle, 12 bottles per case because of error during packaging in which a A Megasorb B-Complex product was filled into bottles labeled as Glucosamine_Chondroitin MSM.
Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
Failed Release Testing: Coarse Particle Mass for umeclidinium Out of Specification
Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.
FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
Label mix-up and therefore required label information is inaccurate
Undeclared MCT Powder (MCT oil, acacia fiber)
Failed Dissolution Specifications
Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the container is a 0.5mL single-use syringe instead of a 5 mL dropper
OOS for viscosity