Reported Mar 25, 2020 · Terminated

Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 80 tablets per bottle. [NDC

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?

Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 80 tablets per bottle. [NDC

5 of 5 products

Products covered by this recall
#Product as published
1Brand] NDC Basic Care: 0113-7876-27
2NDC CVS Health: 69842-293-27
3NDC Leader: 70000-0375-2
4NDC Up & Up: 11673-876-27
5NDC Walgreens: 0363-1876-27
Lot codes and dates
  • Lots
    • 8CE1643
    • 8DE1370
    • 8DE1768
    • 8EE1560
    • 8FE1452
    • 8GE1341
    • 8HE1223
    • 8KE2832
    • 8KE2246
    • 8ME2725
    • 9AE2835
    • 9CE3378
    • 9DE2748
    • 9EE2637
    • 9FE2976
    • 9GE2795
    • 9GE3228
    • 9HE3617

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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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, 7:03 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.