FDA Food recall F-0820-2017
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701
- FDA Food
- Class III
- terminated
- Published 2016-12-28
On 2016-12-28 the FDA classified a Class III recall of Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701 by Hi Tech Pharmacal, citing the firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0820-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-08-25 |
| Published | 2016-12-28 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Hi Tech Pharmacal |
| Distribution | CA, FL, ID, IL, LA, MI, NC, NJ, NY, OH, PA, PR, VT |
Product
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701
Reason
The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.
Identifiers
| code_info | Lot 619618 (Exp. 01/2015) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0820-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.