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Class II: temporary or reversible health riskTerminated

Nestle Product Technology Center - Nestle Health Science Douglas Labs Stress-B-Plus Dietary Supplement Recall

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

Nestle Product Technology Center - Nestle Health Science · Bridgewater, NJ

Risk level
Class II
Reported by FDA
Nov 27, 2024
Recall ID
F-0139-2025
Check your lot numberHow we source this data

Summary

Nestle Product Technology Center - Nestle Health Science recalled Douglas Labs Stress-B-Plus Dietary Supplement starting Oct 7, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0139-2025 on Nov 27, 2024. 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). Status: Terminated.

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 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).

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

Lot numbers, UPCs & expiration codes

Lot Codes: 50335944, 50344396

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0139-2025
Classification
Class II
Status
Terminated
Recall initiated
Oct 7, 2024
FDA report date
Nov 27, 2024
Quantity
3,269 bottles in market
Recall type
Voluntary: Firm initiated
Recalling firm
Nestle Product Technology Center - Nestle Health Science

Original FDA data

Every field from FDA enforcement report F-0139-2025, exactly as published.

Show all FDA fields
City
Bridgewater
State
NJ
Status
Terminated
Country
United States
Event ID
95519
Address
1007 Us Highway 202/206 Bldg Jr2
Code information
Lot Codes: 50335944, 50344396
Postal code
08807-1275
Report date
Nov 27, 2024
Product type
Food
Recall number
F-0139-2025
Classification
Class II
Recalling firm
Nestle Product Technology Center - Nestle Health Science
Product quantity
3,269 bottles in market
Termination date
Jun 24, 2026
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).
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
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
Recall initiation date
Oct 7, 2024
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Nov 17, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0139-2025, published Nov 27, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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