Hi-Tech Pharmacal Co., Inc. recalls FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY 11

Recalled March 11, 2015 · FDA recall F-1380-2015 · Hi-Tech Pharmacal

Hazard

Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120. · FDA Class II

Units

581 units

Sold at

NJ, OH, TX, LA, and Puerto Rico

Description

Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.

Product

FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY 11701

Manufacturer(s)

Hi-Tech Pharmacal Co., Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →