Severity
Moderate
FDA Drug recall · Reported June 7, 2023
CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Denison Pharmaceuticals, LLC recalled Safe tussin PM, NIGHT TIME Cough Relief, (Dextromethorphan HBr, USP 7.5mg, Doxylamine Suc… - a moderate-severity action.
Safe tussin PM, NIGHT TIME Cough Relief, (Dextromethorphan HBr, USP 7.5mg, Doxylamine Suc… was recalled by Denison Pharmaceuticals, LLC in June 7, 2023. Reason: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.. Check the official notice for the remedy. Verify recall #D-0775-2023 with the FDA Drug before acting.
The recall
Denison Pharmaceuticals, LLC issued this moderate-severity FDA Drug recall-CGMP Deviations: Use of non-food grade lubricant in mixing vessel..
Sourced from official FDA Drug enforcement records. Verify recall #D-0775-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0775-2023) was formally reported on June 7, 2023, with the manufacturer initiating the action on May 3, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. Denison Pharmaceuticals, LLC is listed as the recalling firm, operating out of Lincoln, RI. Federal records list the affected scope as 13,968 bottles.
The documented reason for this recall is: CGMP Deviations: Use of non-food grade lubricant in mixing vessel. Distribution data in the federal record shows the product reached: Product was distributed 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 - 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 - 25,126 food 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
13,968 bottles
Related Recalls
6
0 from same agency
Safe tussin PM, NIGHT TIME Cough Relief, (Dextromethorphan HBr, USP 7.5mg, Doxylamine Succinate 3.125mg), 4.0 FL OZ (118mL) bottle, Kramer Laboratories , Inc. Bridgewater, NJ 08807.
CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0775-2023 |
| Date reported | June 7, 2023 |
| Date initiated | May 3, 2023 |
| Recalling firm | Denison Pharmaceuticals, LLC |
| Firm location | Lincoln, RI |
| Affected scope | 13,968 bottles |
| Distribution | Product was distributed 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 June 7, 2023. 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.