FDA Food recall F-1132-2016
Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules
- FDA Food
- Class II
- terminated
- Published 2016-05-04
On 2016-05-04 the FDA classified a Class II recall of Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules by Now Foods, citing undeclared soy lecithin in 5 dietary supplements.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1132-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-18 |
| Published | 2016-05-04 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Now Foods |
| Distribution | 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, PR, SC, SD, TN, TX, VA, VT, WA, WI, WV, WY |
Product
Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules. The bottle has a blue cap and white lettering.
Reason
Undeclared soy lecithin in 5 dietary supplements.
Identifiers
| code_info | Lot# 1961645, Batch# 579391 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1132-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.