Recall map → All recalls → F-0139-2025
Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944 and 50344396. Expiration Date 04/11/2026 Nestle Product Technology Center - Nestle Health Science · reported 2024-11-27
Terminated This recall has been closed out by the agency.
- Reason for recall
- Nestle Health Science (NHS U.S., LLC) is initiating a recall of Douglas Labs Stress-B-Plus Dietary Supplement Tablets, 90 tablets per bottle. The bottle is white and made of plastic. Lot Numbers 50335944,50344396, expiration date 04/11/2026. The product is being recalled because of Incorrect formulation manufactured vs label claims. Product was manufactured with Niacin (as Nicotinic acid) and supplement facts panel states contains Niacin (as Niacinamide).
- Classification
- Class II
- Recall initiated
- 2024-10-07
- Reported by the agency
- 2024-11-27
- Closed out (terminated)
- 2026-06-24
- Recalling firm
- Nestle Product Technology Center - Nestle Health Science
Bridgewater, NJ
United StatesThis is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
- Distribution (the agency's own words)
- AK,AZ,CA,CO,DE,FL,GA,IA,ID,IL,IN,KS,KY,LA,MA,MD,MI,MN,MO,NC,NH,NJ,NM,NY,OH,OK,OR,PA,SD,TN,TX,VA,WA,WI,WV
- States we parsed from that text
- AK AZ CA CO DE FL GA IA ID IL IN KS KY LA MA MD MI MN MO NC NH NJ NM NY OH OK OR PA SD TN TX VA WA WI WV
The agency named these states. Parse method explicit_state_list, confidence high.
- Food category
- Dietary supplementsderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
- Recall type
- Voluntary: Firm initiated
- Recall number
- F-0139-2025
View this record at the agency source →
This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.