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Hi-Tech Pharmacal Co., Inc.

3 recall records on file.

2016

2 records

Class IIITerminatedRecall F-0817-2017

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

Reason for recall

Out-of-specification results for pH.

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Event ID
68873
Code info
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).
Product quantity
22,872 bottles
Distribution pattern
CA, FL, ID, IL, LA, MI, MN, NC, ND, NJ, NY, OH, PA, SC, VT and Puerto Rico
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
369 Bayview Ave, N/A, Amityville, NY, United States
Recall initiation date
07/28/2014
Center classification date
12/20/2016
Termination date
09/08/2017
Class IIITerminatedRecall F-0820-2017

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

Reason for recall

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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Event ID
69095
Code info
Lot 619618 (Exp. 01/2015)
Product quantity
7692 bottles
Distribution pattern
CA, FL, ID, IL, LA, MI, NC, NJ, NY, OH, PA, VT, and Puerto Rico
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
369 Bayview Ave, N/A, Amityville, NY, United States
Recall initiation date
08/25/2014
Center classification date
12/21/2016
Termination date
09/08/2017

2015

1 record

Class IITerminatedRecall F-1380-2015

Product description

FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY 11701

Reason for recall

Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.

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Event ID
70097
Code info
Lot 62110, exp. date 04/2015
Product quantity
581 units
Distribution pattern
NJ, OH, TX, LA, and Puerto Rico
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
369 Bayview Ave, N/A, Amityville, NY, United States
Recall initiation date
12/23/2014
Center classification date
03/03/2015
Termination date
05/08/2017