Class IIITerminated in FDA datasetJul 28, 2014

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

Out-of-specification results for pH.

Check the codes ↓

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 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).

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

FDA source record · F-0817-2017

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.