Rx CHOICE brand LIQUID VITAMIN C — Class III food recall F-0817-2017
Terminated recall by Hi-Tech Pharmacal Co., Inc., reported 2016-12-28, distributed in CA, FL, ID, IL, LA, MI, MN, NC…. Out-of-specification results for pH.
| Recall number | F-0817-2017 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hi-Tech Pharmacal Co., Inc., Amityville, NY, United States |
| Recall initiated | 2014-07-28 |
| Classified | 2016-12-20 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2017-09-08 |
| Distributed | CA, FL, ID, IL, LA, MI, MN, NC, ND, NJ, NY, OH, PA, PR, SC, VT |
| Quantity | 22,872 bottles |
| NDC | 50383-0167-16 |
| Lot numbers | 618283, 620151, 620915, 623407 |
| Expiration dates | 2015-01, 2015-03, 2015-04, 2015-07, 2015-09, 2015-12, 2016-02, 2016-04, 2016-05 |
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 for recall
Out-of-specification results for pH.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0817-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.