RECALLING FIRM / COMPANY
Hi-Tech Pharmacal Co., Inc. recalls
No records with a clear FDA ongoing status found in this snapshot.As of September 18, 2026 · Source export September 16, 2026
These records name this recalling firm. Retailer mentions under other firms are available through search.
Same product name.
Different batch.
Check the label.
Different batch.
Check the label.
Latest Hi-Tech Pharmacal Co., Inc. recall records
3 recall recordsPage 1 of 1
Class II
FERROUS SULFATE ELIXIR 220 mg/5 mL
Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.
OtherView details →Class III
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY…
The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.
OtherView details →Class III
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY…
Out-of-specification results for pH.
OtherView details →Found your product? Now check the codes.
Same product name. Different batch. Details matter.