"SUNDIAL***ETHIOPIAN ABISH (FENNUGREEK SEED POWDER.)***"
Reported: September 9, 2020 Initiated: June 30, 2020 #F-1502-2020
Product Description
"SUNDIAL***ETHIOPIAN ABISH (FENNUGREEK SEED POWDER.)***"
Reason for Recall
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Details
- Recalling Firm
- Sundial Herbal Products
- Units Affected
- Unknown
- Distribution
- NY
- Location
- Bronx, NY
Frequently Asked Questions
What product was recalled? ▼
"SUNDIAL***ETHIOPIAN ABISH (FENNUGREEK SEED POWDER.)***". Recalled by Sundial Herbal Products. Units affected: Unknown.
Why was this product recalled? ▼
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 9, 2020. Severity: Moderate. Recall number: F-1502-2020.
Related Recalls
FDA Drug Moderate
Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-count bottle, Rx Only, Manufactured by: U…
Unichem Pharmaceuticals USA Inc. · 2026-02-11
FDA Drug Critical
Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San…
Green Lumber Holdings, LLC · 2026-02-11
FDA Drug Moderate
Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle, Rx only, Manufactured by: Granules India Limited, Hyderabad, 500…
Granules Pharmaceuticals Inc. · 2026-02-11
FDA Drug Critical
Diclofenac Sodium, Topical Gel, 3%, 100 g, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1…
SUN PHARMACEUTICAL INDUSTRIES INC · 2026-02-11
FDA Drug Critical
Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt. Ltd., Ahmedabad, India UPC 8 904218 700313
HANDELNINE GLOBAL LLC · 2026-02-11