Class IITerminated in FDA datasetRecall initiated Oct 7, 2024

Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle.

Recalling firm: Nestle Product Technology Center - Nestle Health Science

Why it was recalled

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…

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: Jun 24, 2026.

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ProductDouglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944 and 50344396. Expiration Date 04/11/2026

FDA code information

Lot Codes: 50335944, 50344396

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
expiration04/11/2026bottle. UPC # 10539 97452, Lot Numbers ,50335944 and 50344396. Expiration Date 04/11/2026
lot50335944Lot Codes: 50335944, 50344396
lot50344396Lot Codes: 50335944, 50344396

Original FDA recall reason

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).

Recall details

Recall number
F-0139-2025
Event ID
95519
FDA status
Terminated
Initiated
Oct 7, 2024
Reported
Nov 27, 2024
Classified
Nov 17, 2024
Terminated
Jun 24, 2026
Quantity
3,269 bottles in market
Location
Bridgewater, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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

FDA source record · F-0139-2025

Data updated September 16, 2026. View official FDA data ↗

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