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 1 GE2743, GE4570, GG0536, Exp 9/30/2018 2 GE3445, GG4810, Exp 11/30/2018 3 A38M, Exp 12/31/2018 4 K63J, Exp 4/30/2018 5 H24T, Exp 5/31/2018 6 RS4U, M721601MA, Exp 7/31/2018 7 379H, Exp 8/31/2018 8 A93E, AE2S, Exp 10/31/2018 9 GB7D, GS5B, M801001MA, M807901MA, M807902MA, exp 11/30/2019 10 D88E, Exp 11/30/2020 2-bottle cartons lot#: GJ0440, Exp 1/31/2019 11 LE6J, Exp 7/31/2018 12 A93E, Exp 10/31/2018 3-bottle cartons lot#: 17D19N, Exp 8/31/2018 13 1GE2743, GE4570, GG0536, Exp 9/30/2018 14 GA8391, Exp 10/31/2018 15 GE3445, GA6310, Exp 11/30/2018 16 GG1094, GH1913, GH8818, M703002EH, M703003EH, M703004EH, M703006EH, M703007EH, M703008EH, M713101EH, M707401MB, M707402MB, M707403MB, M707404MB, M707405MB, M707406MB, M721201MB, M717001MA, M717002MA, Exp 1/31/2018 17 AF5C, AK2T, AV5T, M713102EH, M713104EH, M716001EH, M716002EH, M716003EH, M716004EH, M716005EH, M721202MB, M721203MB, M721204MB, M717003MA, M717004MA, M717005MA, M717006MA, Exp 4/30/2019 18 FL8P, FM4K, M720505EH, M720507EH, M720508EH, M720509EH, M721205MB, M721206MB, M721207MB, Exp 5/31/2019 19 P77N, P77P, PN3Y, R72E, Exp 8/31/2019 20 728J, 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.
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