WHY THIS PRODUCT IS LISTED
Other / see reason
Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.
Product description & recall reason
The recall record describes “FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY …”; the source reports: “Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.”
Based on the official recall record; packaging and sales claims have not been verified. Verify with the official source ↗
Identify the product
- Product description
- FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY 11701
- Brand
- Not supplied by this source
- Lot, batch, UPC & other codes
- Lot 62110, exp. date 04/2015
- Quantity
- 581 units
Where it came from & where it went
- Recalling firm
- Hi-Tech Pharmacal Co., Inc.
- Recalling firm address
- 369 Bayview Ave; N/A; Amityville; NY; 11701-2801; United States
- Product production / origin location
- Not supplied by this source
- Distribution — source wording
- NJ, OH, TX, LA, and Puerto Rico
States identified in the source
Louisiana, New Jersey, Ohio, Puerto Rico, Texas
State matching is derived from the source’s distribution wording, which may be incomplete. The recalling company’s address is not used as the distribution location.
A recalling firm’s address is not necessarily where the food was grown or manufactured. Distribution can change; check the official notice.