Severity
Moderate
FDA Drug recall · Reported July 20, 2022
Labeling: Label Mix-Up-The primary label on the front of the bottles have Hydrogen Peroxide affixed to the front and back of the containers. However, the product inside the bottle…
Vi-Jon, LLC recalled Hydrogen Peroxide Topical Solution, USP, 32 fl. oz. (1 QT) 946 mL, Distributed by: CVS Ph… - a moderate-severity action.
Hydrogen Peroxide Topical Solution, USP, 32 fl. oz. (1 QT) 946 mL, Distributed by: CVS Ph… was recalled by Vi-Jon, LLC in July 20, 2022. Reason: Labeling: Label Mix-Up-The primary label on the front of the bottles have Hydrogen Peroxide affixed to the fr…. Check the official notice for the remedy. Verify recall #D-1191-2022 with the FDA Drug before acting.
The recall
Vi-Jon, LLC issued this moderate-severity FDA Drug recall-Labeling: Label Mix-Up-The primary label on the front of the bottles have Hydrogen Peroxide affixed to the fr….
Sourced from official FDA Drug enforcement records. Verify recall #D-1191-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-1191-2022) was formally reported on July 20, 2022, with the manufacturer initiating the action on June 24, 2022. It is classified under Moderate severity (Class II), with a current status of Terminated. Vi-Jon, LLC is listed as the recalling firm, operating out of Smyrna, TN. Federal records list the affected scope as 36,840 bottles.
The documented reason for this recall is: Labeling: Label Mix-Up-The primary label on the front of the bottles have Hydrogen Peroxide affixed to the front and back of the containers. However, the product inside the bottle is 70% Isopropyl Alcohol. Distribution data in the federal record shows the product reached: USA 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 - 3,731 children & baby products 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
36,840 bottles
Related Recalls
6
0 from same agency
Hydrogen Peroxide Topical Solution, USP, 32 fl. oz. (1 QT) 946 mL, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, NDC 59779-871-45, UPC 0-50428-40950-3
Labeling: Label Mix-Up-The primary label on the front of the bottles have Hydrogen Peroxide affixed to the front and back of the containers. However, the product inside the bottle is 70% Isopropyl Alcohol.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-1191-2022 |
| Date reported | July 20, 2022 |
| Date initiated | June 24, 2022 |
| Recalling firm | Vi-Jon, LLC |
| Firm location | Smyrna, TN |
| Affected scope | 36,840 bottles |
| Distribution | USA 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.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 July 20, 2022. 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.