Hi-Tech Pharmacal Co., Inc. — recall history

Every FDA and USDA recall we hold for Hi-Tech Pharmacal Co., Inc.. This is a record of published agency notices, not an assessment of the company: a recall is often the result of a firm's own testing and voluntary action, and firms that test more thoroughly may appear here more often.

Class IIFDA23 Dec 2014LA, NJ, OH, PR +1

Hi-Tech Pharmacal Co., Inc. recalls FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMAC (Class II)

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

Class IIIFDA25 Aug 2014CA, FL, ID, IL +9

Hi-Tech Pharmacal Co., Inc. recalls Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACA (Class III)

The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.

Class IIIFDA28 Jul 2014CA, FL, ID, IL +12

Hi-Tech Pharmacal Co., Inc. recalls Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACA (Class III)

Out-of-specification results for pH.