FDA Food EnforcementOther / 其他

Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701

Recall F-0820-2017Published 2016-12-28Company Hi-Tech Pharmacal Co., Inc.

Reason / 召回原因The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.

Distribution / 销售地区CA, FL, ID, IL, LA, MI, NC, NJ, NY, OH, PA, VT, and Puerto Rico

Code information / 批次信息Lot 619618 (Exp. 01/2015)

Official-information notice / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.

Official record details

官方记录详情：以原始机构公告为准

Recall number / 召回编号

F-0820-2017

Classification / 风险等级

Other / 其他

Published / 发布时间

2016-12-28

Recalling firm / 召回企业

Hi-Tech Pharmacal Co., Inc.

Product description / 产品描述

Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

Lot 619618 (Exp. 01/2015)

Product quantity / 产品数量

7692 bottles

Distribution / 销售地区

CA, FL, ID, IL, LA, MI, NC, NJ, NY, OH, PA, VT, and Puerto Rico

Reason for recall / 召回原因

The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.

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Last synchronized: 2026-08-09. Recall Radar does not replace agency guidance.