Data Foundry

Drug recalls 2018

Prevacid 24HR — Class II drug recall D-0088-2019

Terminated recall by GLAXOSMITHKLINE NEBRASKA, reported 2018-10-17, distributed nationwide. CGMP deviations

Recall numberD-0088-2019
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmGLAXOSMITHKLINE NEBRASKA, Lincoln, NE, United States
Recall initiated2018-09-26
Classified2018-10-23
Reported by FDA2018-10-17
Terminated2020-11-06
DistributedNationwide (US)
Quantity5,548,673 bottles
Reason classescgmp
NDC00067-6286-14, 00067-6286-28, 00067-6286-42
Lot numbers17D19N, 1GE2743, 2-BOTTLE, 3-BOTTLE, 379H, 728J, 728K, 728L, 8E6T, A38M, A93E, AE2S, AF5C, AK2T, AV5T, BR4Y, D88E, FL8P, FM4K, FN2N, GA6310, GA8391, GB7D, GE2743, GE3445, GE4570, GG0536, GG1094, GG4810, GH1913, GH8818, GJ0440, GS5B, H24T, H43X, HT4P, K63J, LE6J, M703002EH, M703003EH and 51 more
Expiration dates2018-01-31, 2018-04-30, 2018-05-31, 2018-07-31, 2018-08-31, 2018-09-30, 2018-10-31, 2018-11-30, 2018-12-31, 2019-01-31, 2019-04-30, 2019-05-31, 2019-08-31, 2019-10-31, 2019-11-30, 2020-11-30, 2021-01-31

Product

Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle (NDC: 0067-6286-14), 2 bottles (NDC: 0067-6286-28) or 3 bottles (NDC: 0067-6286-42), Over-the-counter, Distributed By: GSK Consumer Healthcare, Warren, NJ 07059.

Reason for recall

CGMP deviations

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-0088-2019. 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.