Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701
Recalling firm: Hi-Tech Pharmacal Co., Inc.
Why it was recalled
The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.
The exact product
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot 619618 (Exp. 01/2015)
Recall details
- Recall number
- F-0820-2017
- Event ID
- 69095
- FDA status
- Terminated
- Initiated
- Aug 25, 2014
- Reported
- Dec 28, 2016
- Classified
- Dec 21, 2016
- Terminated
- Sep 8, 2017
- Quantity
- 7692 bottles
- Location
- Amityville, NY, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
CA, FL, ID, IL, LA, MI, NC, NJ, NY, OH, PA, VT, and Puerto Rico
FDA source record · F-0820-2017
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.