Severity
Low
FDA Drug recall · Reported January 15, 2020
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
The recall
Idelle Labs issued this low-severity FDA Drug recall — Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the prod….
Sourced from official FDA Drug enforcement records. Verify recall #D-0785-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0785-2020) was formally reported on January 15, 2020, with the manufacturer initiating the action on November 20, 2019. It is classified under Low severity (Class III), with a current status of Terminated. Idelle Labs is listed as the recalling firm, operating out of El Paso, TX. Federal records list the affected scope as Unknown.
The documented reason for this recall is: Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product. Distribution data in the federal record shows the product reached: Nationwide in the USA. 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, 1 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 — 1,052 cosmetics & personal care recalls on record
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified low severity.
Severity
Low
Affected scope
Unknown
Related Recalls
6
1 from same agency
SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5514-1 UPC 8 83484 717936 6 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0785-2020 |
| Date reported | January 15, 2020 |
| Date initiated | November 20, 2019 |
| Recalling firm | Idelle Labs |
| Firm location | El Paso, TX |
| Affected scope | Unknown |
| Distribution | Nationwide in the USA |
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
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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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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Drug, reported January 15, 2020.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.