Severity
Moderate
FDA Food recall · Reported February 10, 2016
Madison One Acme, Inc. dba Solstice Medicine is recalling Tong Ren Tang Shenjing Shuairuo Wan because it contains the unapproved dietary ingredient human placenta which may transm…
Madison One Acme Inc recalled Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills UPC Code: 6 904579 … - a moderate-severity action.
Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills UPC Code: 6 904579 … was recalled by Madison One Acme Inc in February 10, 2016. Reason: Madison One Acme, Inc. dba Solstice Medicine is recalling Tong Ren Tang Shenjing Shuairuo Wan because it cont…. Check the official notice for the remedy. Verify recall #F-0526-2016 with the FDA Food before acting.
The recall
Madison One Acme Inc issued this moderate-severity FDA Food recall-Madison One Acme, Inc. dba Solstice Medicine is recalling Tong Ren Tang Shenjing Shuairuo Wan because it cont….
Sourced from official FDA Food enforcement records. Verify recall #F-0526-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0526-2016) was formally reported on February 10, 2016, with the manufacturer initiating the action on January 7, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Madison One Acme Inc is listed as the recalling firm, operating out of Los Angeles, CA. Federal records list the affected scope as 12500.
The documented reason for this recall is: Madison One Acme, Inc. dba Solstice Medicine is recalling Tong Ren Tang Shenjing Shuairuo Wan because it contains the unapproved dietary ingredient human placenta which may transmit disease. Distribution data in the federal record shows the product reached: U.S. distribution to the following; CA, CO, AZ, WA, OH, NC, AL, NJ, CT, IL, HI, NY, TX, OR, FL, GA, NM, VA, MD, LA, MA, MI, ME, MN, PA, NC, AK, KS Foreign distribution to the following: CA. 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
12500
Related Recalls
6
6 from same agency
Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills UPC Code: 6 904579 129602 Distributed by: Solstice Medicine Company
Madison One Acme, Inc. dba Solstice Medicine is recalling Tong Ren Tang Shenjing Shuairuo Wan because it contains the unapproved dietary ingredient human placenta which may transmit disease.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0526-2016 |
| Date reported | February 10, 2016 |
| Date initiated | January 7, 2016 |
| Recalling firm | Madison One Acme Inc |
| Firm location | Los Angeles, CA |
| Affected scope | 12500 |
| Distribution | U.S. distribution to the following; CA, CO, AZ, WA, OH, NC, AL, NJ, CT, IL, HI, NY, TX, OR, FL, GA, NM, VA, MD, LA, MA, MI, ME, MN, PA, NC, AK, KS Foreign distribution to the following: CA |
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 February 10, 2016. 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.