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.
Out-of-specification results for pH.
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 618283 (Exp. 01/2015), Lot 620151 (Exp. 03/2015), Lot 623407 (Exp. 09/2015) --- EXTENSION: Lots 620915 (Expiry 04/2015), 622298 (Exp. 07/2015), 624881 (Exp. 12/2015), 625981 (Exp. 02/2016), 626967 (Exp. 04/2016), 627676 (Exp. 05/2016).
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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
Out-of-specification results for pH.
Recall details
- Recall number
- F-0817-2017
- Event ID
- 68873
- FDA status
- Terminated
- Initiated
- Jul 28, 2014
- Reported
- Dec 28, 2016
- Classified
- Dec 20, 2016
- Terminated
- Sep 8, 2017
- Quantity
- 22,872 bottles
- Location
- Amityville, NY, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
CA, FL, ID, IL, LA, MI, MN, NC, ND, NJ, NY, OH, PA, SC, VT and Puerto Rico
Data updated September 16, 2026. View official FDA data ↗
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