Hi-Tech Pharmacal Co Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ recall — FDA F-0817-2017
Out-of-specification results for pH.
Overview of recall records associated with Hi-Tech Pharmacal Co., Inc., including dates, categories and classifications where available.
Classification mix: Class III: 5, Class II: 2.
Out-of-specification results for pH.
The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.
Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.
Failed Impurity/Degradation Specification; out-of-specification result for one individual unknown impurity at the 24-month room temperature stability test station.
Subpotent; phenylephrine HCl
Labeling: Label Mix-up; some cartons labeled as Clobetasol Propionate Cream USP contain tubes labeled as Clobetasol Propionate Gel USP. The actual product in the tube is Clobetasol…
Subpotent Drug: The product/lot is out-of-specification (OOS) for the assay of acetic acid at the 18-month test station.
This page summarizes recall records in which the official source identifies Hi-Tech Pharmacal Co., Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.