Data / Product recalls / Hi-Tech Pharmacal Co., Inc.
Hi-Tech Pharmacal Co., Inc.: 3 recalls from 2015 to 2016 (FDA)
Hi-Tech Pharmacal Co., Inc., Amityville, NY, is named in 3 recalls from 2015 to 2016: all from the FDA. The latest, on December 28, 2016, covers Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY.... Hazard: The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label. Source: FDA F-0820-2017.
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- Country
- United States
- Location
- Amityville, NY
- Agencies
- U.S. Food and Drug Administration
- First recall
- March 11, 2015
- Latest recall
- December 28, 2016
Recalls
Each recall is listed once, with the role this firm has in it. Roles: recalling firm (3).
| Date | Agency | Product | Hazard | Units | Remedy | Sold at | Role | Source |
|---|---|---|---|---|---|---|---|---|
| December 28, 2016 | FDA | Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701 | The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label. | 7692 bottles | Voluntary recall, Class III, terminated | Recalling firm | accessdata.fda.gov | |
| December 28, 2016 | FDA | Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701 | Out-of-specification results for pH. | 22,872 bottles | Voluntary recall, Class III, terminated | Recalling firm | accessdata.fda.gov | |
| March 11, 2015 | FDA | FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY 11701 | Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120. | 581 units | Voluntary recall, Class II, terminated | Recalling firm | accessdata.fda.gov |
By agency
| Agency | Recalls | Latest |
|---|---|---|
| U.S. Food and Drug Administration | 3 | December 28, 2016 |
Categories
| Category | Recalls |
|---|---|
| Dietary supplements | 2 |
Where each agency publishes its recalls
Updated December 28, 2016. Read from U.S. Food and Drug Administration recall data. CC0 1.0 (openFDA). Recalls are as the agencies published them: the CPSC, FDA (food enforcement reports) and NHTSA. A firm is one firm only when its exact name and country match; the CPSC and FDA print no firm ID. Stores are listed only when the agency's sold-at text names them, and an agency often adds that more stores sold the product. Categories are grouped by SpecStream from the words in the agency's title and product text. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.