FDA recall record

Perrigo Company PLC Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 24 recall — FDA D-1018-2020

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Class IIclassification
D-1018-2020official record ID
Mar 25, 2020report date

Recall record at a glance

Official recordD-1018-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPerrigo Company PLC
Report dateMar 25, 2020
Recall initiation dateOct 23, 2019
LocationAllegan, MI, United States

Official product description

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 24 tablets per bottle. [Brand, NDC] NDC Being Well: 46994-852-62; NDC Care One 41520-392-02; NDC CVS Health: 59779-540-02; NDC DG Health: 55910-852-02; NDC Equaline: 41163-852-62; NDC Equate: 49035-608-02; NDC Exchange Select: 55301-852-02; NDC Family Wellness: 55319-852-02; NDC Good Neighbor Pharmacy: 46122-224-62; NDC Good Sense 0113-0852-62; NDC Harris Teeter: 69256-041-62; NDC Health Mart 49348-109-04; NDC Kroger 30142-600-02; NDC Major 0904-6716-24; NDC Meijer: 41250-852-02; NDC Publix: 56062-099-02; NDC Rite Aid 11822-0852-5; NDC Select 7: 10202-852-62; NDC Shop Rite 41190-852-62; NDC Shopko: 37012-852-62; NDC Signature Care: 21130-116-02; NDC Sound Body: 50594-852-02; NDC Sunmark: 62011-0282-1; NDC Topcare: 36800-852-02; NDC Up & Up: 11673-023-02; NDC Walgreens: 0363-0852-62

Why the product was recalled

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Distribution information

Nationwide USA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

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About this record

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