Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL…
Recalling firm: Hi-Tech Pharmacal Co., Inc.
The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 8, 2017.
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FDA code information
Lot 619618 (Exp. 01/2015)
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Full FDA record and distribution details
Original product description
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701
Original FDA recall 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.
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
Data updated September 16, 2026. View official FDA data ↗
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