Severity
Moderate
FDA Drug recall · Reported November 20, 2019
GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).
Apotex Inc. recalled Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets, USP 75 mg/Acid Reducer 30 Table… - a moderate-severity action.
Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets, USP 75 mg/Acid Reducer 30 Table… was recalled by Apotex Inc. in November 20, 2019. Reason: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).. Check the official notice for the remedy. Verify recall #D-0315-2020 with the FDA Drug before acting.
The recall
Apotex Inc. issued this moderate-severity FDA Drug recall-GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA)..
Sourced from official FDA Drug enforcement records. Verify recall #D-0315-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0315-2020) was formally reported on November 20, 2019, with the manufacturer initiating the action on September 24, 2019. It is classified under Moderate severity (Class II), with a current status of Completed. Apotex Inc. is listed as the recalling firm, operating out of North York, N/A. Federal records list the affected scope as 42,873 bottles.
The documented reason for this recall is: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA). Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
42,873 bottles
Related Recalls
6
5 from same agency
Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets, USP 75 mg/Acid Reducer 30 Tablets NDC 0363-1029-03 Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015
GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Completed |
| Recall number | D-0315-2020 |
| Date reported | November 20, 2019 |
| Date initiated | September 24, 2019 |
| Recalling firm | Apotex Inc. |
| Firm location | North York, N/A |
| Affected scope | 42,873 bottles |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported November 20, 2019. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.