Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules. The…
Recalling firm: NOW Foods
Undeclared soy lecithin in 5 dietary supplements.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 21, 2017.
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FDA code information
Lot# 1961645, Batch# 579391
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Full FDA record and distribution details
Original product description
Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules. The bottle has a blue cap and white lettering.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| batch | 579391 | Lot# 1961645, Batch# 579391 |
| lot | 1961645 | Lot# 1961645, Batch# 579391 |
Original FDA recall reason
Undeclared soy lecithin in 5 dietary supplements.
Recall details
- Recall number
- F-1132-2016
- Event ID
- 73695
- FDA status
- Terminated
- Initiated
- Mar 18, 2016
- Reported
- May 4, 2016
- Classified
- Apr 22, 2016
- Terminated
- Jul 21, 2017
- Quantity
- 12 bottles
- Location
- Bloomingdale, IL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV, WY and PR. The one foreign consignee is Natulab in Japan.
Data updated September 16, 2026. View official FDA data ↗
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