Reported Mar 25, 2020 · Terminated

Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 150 tablets per bottle. [NDC: Brand] NDC H.E.B.:…

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, 150 tablets per bottle. [NDC: Brand] NDC H.E.B.: 37808-876-47
  • NDC Equate49035-876-47
Lot codes and dates
  • Lots
    • 8CE1644
    • 8CE1645
    • 8DE1401
    • 8DE1402
    • 8DE1403
    • 8DE1769
    • 8DE1773
    • 8EE1561
    • 8EE1562
    • 8FE1453
    • 8FE1454
    • 8GE1342
    • 8HE1224
    • 8KE2248
    • 8KE2833
    • 8JE1918
    • 8KE2247
    • 8ME2727
    • 8ME2729
    • 9DE2750
    • 9AE2836
    • 9AE2837
    • 9CE3403
    • 9CE3404
    • 9DE2749
    • 9EE2638
    • 9FE2977
    • 9GE2796
    • 9GE3229

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, 6:25 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.