Severity
Moderate
FDA Food recall · Reported November 27, 2013
Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi fo…
Pharmavite Corporation recalled Multi for Her 50+ (Full Strength Mini and Multi softgels) 24 units per master case. … - a moderate-severity action.
Multi for Her 50+ (Full Strength Mini and Multi softgels) 24 units per master case. … was recalled by Pharmavite Corporation in November 27, 2013. Reason: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitami…. Check the official notice for the remedy. Verify recall #F-0186-2014 with the FDA Food before acting.
The recall
Pharmavite Corporation issued this moderate-severity FDA Food recall-Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitami….
Sourced from official FDA Food enforcement records. Verify recall #F-0186-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0186-2014) was formally reported on November 27, 2013, with the manufacturer initiating the action on September 9, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Pharmavite Corporation is listed as the recalling firm, operating out of Northridge, CA. Federal records list the affected scope as 182,698 bottles.
The documented reason for this recall is: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi for Her, Multi for Her 50+, Multi for Him,… Distribution data in the federal record shows the product reached: US nationwide. No International.. 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, 6 from FDA Food - 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 - 2,002 dietary supplements 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
182,698 bottles
Related Recalls
6
6 from same agency
Multi for Her 50+ (Full Strength Mini and Multi softgels) 24 units per master case. Product labeling reads in part:"NatureMade***DIETARY SUPPLEMENT 60 SOFTGELS***Distributed by: Nature Made Nutritional Products Mission Hills, CA 91346-9606, U.S.A 1-800-276-2878 www.NatureMade.com***"
Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi for Her, Multi for Her 50+, Multi for Him, Multi Complete club size). because recent quality tests indicate that the Vitamins B1 and B12 are losing potency more rapidly than initially expected, and these products are not me
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0186-2014 |
| Date reported | November 27, 2013 |
| Date initiated | September 9, 2013 |
| Recalling firm | Pharmavite Corporation |
| Firm location | Northridge, CA |
| Affected scope | 182,698 bottles |
| Distribution | US nationwide. No International. |
Profile values are sourced directly from the official FDA Food 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 Food 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 Food, reported November 27, 2013. 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.