Dream Body Advanced 400 mg 30 capsules in brown foil packets.
Reported: October 26, 2016 Initiated: July 1, 2016 #D-0108-2017
Product Description
Dream Body Advanced 400 mg 30 capsules in brown foil packets.
Reason for Recall
Marketed without an approved NDA/ANDA: Undeclared sibutramine.
Details
- Recalling Firm
- Dream Body Weight Loss
- Units Affected
- Unknown
- Distribution
- United States
- Location
- Grand Prairie, TX
Frequently Asked Questions
What product was recalled? ▼
Dream Body Advanced 400 mg 30 capsules in brown foil packets.. Recalled by Dream Body Weight Loss. Units affected: Unknown.
Why was this product recalled? ▼
Marketed without an approved NDA/ANDA: Undeclared sibutramine.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 26, 2016. Severity: Moderate. Recall number: D-0108-2017.
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