Reported Mar 25, 2020 · Terminated

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care:…

Perrigo Company PLC

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: Perrigo Company PLC · 515 Eastern Ave · Allegan, MI · 49010-9070

Is this the product you have?

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care

9 of 9 products

Products covered by this recall
#Product as published
10113-7852-01
2NDC Berkley Jensen: 68391-852-56
3NDC: CVS Health: 59779-540-01
4NDC DG Health: 55910-011-01
5NDC Kirkland: 63981-852-56
6NDC Kroger: 30142-600-56
7NDC Meijer: 41250-852-01
8NDC Rite Aid: 11822-0852-4
9NDC Walgreens: 0363-0852-01
Lot codes and dates
  • Lots

    109 of 109 codes

    • 8CE1446
    • 8DE1740
    • 8FE1238
    • 8FE1794
    • 8GE1964
    • 8JE2159
    • 8ME2546
    • 8ME2547
    • 9BE3011
    • 9CE3854
    • 9DE3158
    • 9FE3340
    • 9HE3445
    • 9JE2663
    • 8AE1779
    • 8BE1414
    • 8DE1199
    • 8DE1200
    • 8DE1532
    • 8EE1321
    • 8FE1239
    • 8FE1346
    • 8FE1793
    • 8HE1516
    • 8KE2563
    • 8KE2563R
    • 8LE2260
    • 9AE2610
    • 9AE2612
    • 9BE3012
    • 9BE3013
    • 9CE3852
    • 9DE3156R
    • 9DE3160
    • 9DE3161
    • 9EE2952
    • 9FE3338
    • 9GE2993
    • 8AV1095
    • 8AV1150
    • 8AV1235
    • 8AV1236
    • 8AV1237
    • 8BV0896
    • 8BV0897
    • 8BV0910
    • 8BV1737
    • 8BV1757
    • 8BV1758
    • 8CV0930
    • 8CV1316
    • 8CV1317
    • 8CV1319
    • 8CV1324
    • 8CV1633
    • 8DV1128
    • 8DV1129
    • 8DV1134
    • 8EV0993
    • 8EV0994

This recall covers 17 products

The agency filed one notice per product. You are reading one of them; the other 16 are below.

4 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 6:36 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.