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Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills recall
Recalled by Madison One Acme Inc · Los Angeles, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
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.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills UPC Code: 6 904579 129602 Distributed by: Solstice Medicine Company
Quantity: 12500
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
SMC Code: TRT10 Lot #2080130
Where it was sold
Alaska Alabama Arizona California Colorado Connecticut Florida Georgia Hawaii Illinois Kansas Louisiana Massachusetts Maryland Maine Michigan Minnesota North Carolina New Jersey New Mexico New York Ohio Oregon Pennsylvania Texas Virginia Washington
FDA's distribution note: 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
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Madison One Acme Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 7, 2016
- In FDA report of
- Feb 10, 2016
- Terminated
- Oct 14, 2016
- FDA recall number
- F-0526-2016 · event 73019
- Official record
- FDA enforcement report search
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