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Nestle Product Technology Center - Nestle Health Science

2 recall records on file.

2024

2 records

Class IITerminatedRecall F-0139-2025

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

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).

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Event ID
95519
Code info
Lot Codes: 50335944, 50344396
Product quantity
3,269 bottles in market
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
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product type
Food
Recalling firm location
1007 Us Highway 202/206 Bldg Jr2, N/A, Bridgewater, NJ, United States
Recall initiation date
10/07/2024
Center classification date
11/17/2024
Termination date
06/24/2026
Class IIITerminatedRecall F-0803-2024

Product description

Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM, 120 Tablets per bottle. Glass Bottle, 12 per Case, Store at room temperature . Product Number -1319

Reason for recall

Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle, 12 bottles per case because of error during packaging in which a A Megasorb B-Complex product was filled into bottles labeled as Glucosamine_Chondroitin MSM.

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Event ID
93707
Code info
Lot/Unit Numbers: 3250UM0704 UPC Codes: 041260351211
Product quantity
612 bottles
Distribution pattern
The recalled product was distributed to the following states: NY, IN, PA, TX, TN, NV
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product type
Food
Recalling firm location
1007 Us Highway 202/206 Bldg Jr2, Bridgewater, NJ, United States
Recall initiation date
12/22/2023
Center classification date
01/26/2024
Termination date
03/26/2024