Reported Oct 17, 2018 · Terminated

Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle…

Glaxosmithkline Nebraska

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GLAXOSMITHKLINE NEBRASKA · 10401 Hwy 6 · Lincoln, NE · 68517-9626

Is this the product you have?

  • Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle
  • in a carton containing 1 bottle (NDC
    • 0067-6286-14)
    • 2
  • bottles (NDC0067-6286-28)
  • or 3 bottles (NDC0067-6286-42), Over-the-counter
  • Distributed ByGSK Consumer Healthcare, Warren, NJ 07059
Lot codes and dates

24 of 24 products

Products covered by this recall
#Product as published
1GE2743, GE4570, GG0536, Exp 9/30/2018
2GE3445, GG4810, Exp 11/30/2018
3A38M, Exp 12/31/2018
4K63J, Exp 4/30/2018
5H24T, Exp 5/31/2018
6RS4U, M721601MA, Exp 7/31/2018
7379H, Exp 8/31/2018
8A93E, AE2S, Exp 10/31/2018
9GB7D, GS5B, M801001MA, M807901MA, M807902MA, exp 11/30/2019
10D88E, Exp 11/30/2020 2-bottle cartons lot#: GJ0440, Exp 1/31/2019
11LE6J, Exp 7/31/2018
12A93E, Exp 10/31/2018 3-bottle cartons lot#: 17D19N, Exp 8/31/2018
131GE2743, GE4570, GG0536, Exp 9/30/2018
14GA8391, Exp 10/31/2018
15GE3445, GA6310, Exp 11/30/2018
16GG1094, GH1913, GH8818, M703002EH, M703003EH, M703004EH, M703006EH, M703007EH, M703008EH, M713101EH, M707401MB, M707402MB, M707403MB, M707404MB, M707405MB, M707406MB, M721201MB, M717001MA, M717002MA, Exp 1/31/2018
17AF5C, AK2T, AV5T, M713102EH, M713104EH, M716001EH, M716002EH, M716003EH, M716004EH, M716005EH, M721202MB, M721203MB, M721204MB, M717003MA, M717004MA, M717005MA, M717006MA, Exp 4/30/2019
18FL8P, FM4K, M720505EH, M720507EH, M720508EH, M720509EH, M721205MB, M721206MB, M721207MB, Exp 5/31/2019
19P77N, P77P, PN3Y, R72E, Exp 8/31/2019
20728J, 728K, 728L, 8E6T, A93E, Exp 10/31/2019
Amount recalled
5,548,673 bottles

Where it was sold

  • Nationwide
  • PR

Why it was recalled

CGMP deviations

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Nov 6, 2020 · Data as of Sep 19, 6:37 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.