FDA recall record

Hi-Tech Pharmacal Co FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC recall — FDA F-1380-2015

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

Class IIclassification
F-1380-2015official record ID
Mar 11, 2015report date

Recall record at a glance

Official recordF-1380-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHi-Tech Pharmacal Co., Inc.
Report dateMar 11, 2015
Recall initiation dateDec 23, 2014
Quantity581 units
LocationAmityville, NY, United States

Official product description

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

Why the product was recalled

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

Distribution information

NJ, OH, TX, LA, and Puerto Rico

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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