Data Foundry

Drug recalls 2015

Hydroxyzine Hydrochloride — Class II drug recall D-1130-2015

Terminated recall by Akorn, Inc., reported 2015-06-17, distributed nationwide. Failed Impurities/Degradation Specifications

Recall numberD-1130-2015
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAkorn, Inc., Lake Forest, IL, United States
Recall initiated2015-04-07
Classified2015-06-09
Reported by FDA2015-06-17
Terminated2017-11-29
DistributedNationwide (US)
Reason classesspecification failure
NDC50383-0796-16
Lot numbers620984, 620987, 621481, 621484, 621752, 621754, 621875, 622239, 622742, 622745, 623371, 623374, 623820, 623823, 624265, 624268, 624824, 624827, 625472, 625475, 625783, 625786, 626447, 626450, 627683, 627797, 627800, 629094, 629097, 629100, 629103, 629928, 629931, 630480, 630483, 630874, 630877, 631513
Expiration dates2015-04, 2015-05, 2015-06, 2015-08, 2015-09, 2015-10, 2015-11, 2016-01, 2016-05, 2016-06, 2016-08, 2016-09, 2016-10, 2016-12

Product

Hydroxyzine Hydrochloride, oral solution, 10 mg per 5 mL, 16 fl oz (473 ml) bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc., Amityville, NY, NDC 50383-0796-16

Reason for recall

Failed Impurities/Degradation Specifications

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1130-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.