Maximum Strength Acid Reducer — Class II drug recall D-1018-2020
Terminated recall by Perrigo Company PLC, reported 2020-03-25, distributed nationwide. CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
| Recall number | D-1018-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Perrigo Company PLC, Allegan, MI, United States |
| Recall initiated | 2019-10-23 |
| Classified | 2020-03-13 |
| Reported by FDA | 2020-03-25 |
| Terminated | 2020-11-06 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp, specification failure |
| NDC | 00113-0852-62, 00363-0852-62, 00904-6716-24, 10202-0852-62, 11673-0023-02, 11822-0852-05, 21130-0116-02, 30142-0600-02, 36800-0852-02, 37012-0852-62, 41163-0852-62, 41190-0852-62, 41250-0852-02, 41520-0392-02, 46122-0224-62, 46994-0852-62, 49035-0608-02, 49348-0109-04, 50594-0852-02, 55301-0852-02, 55319-0852-02, 55910-0852-02, 56062-0099-02, 59779-0540-02, 62011-0282-01 and 1 more |
| Lot numbers | 8AE1743, 8BE1340, 8CE1314, 8CE1315, 8CE1549, 8CE1778, 8DE1096, 8DE1128, 8DE1313, 8DE1530, 8DE1640, 8DE1721, 8EE1117, 8EE1234, 8EE1299, 8EE1452, 8EE1452R, 8EE1699, 8FE1634, 8GE1528, 8GE1833, 8GE1835, 8HE1337, 8HE1465, 8JE2162, 8JE2199, 8KE2495, 8KE2496, 8LE2169, 8LE2172, 8LE2173, 8LE2288, 8LE2380, 8LE2592, 8LE2593, 8ME3124, 8ME3125, 9BE2772, 9BE2773, 9BE2774 and 25 more |
Product
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
Reason for recall
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1018-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.