Solgar — Class III food recall F-0803-2024
Terminated recall by Nestle Product Technology Center - Nestle Health Science, reported 2024-02-07, distributed in IN, NV, NY, PA, TN, TX. Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle,
| Recall number | F-0803-2024 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nestle Product Technology Center - Nestle Health Science, Bridgewater, NJ, United States |
| Recall initiated | 2023-12-22 |
| Classified | 2024-01-26 |
| Reported by FDA | 2024-02-07 |
| Terminated | 2024-03-26 |
| Distributed | IN, NV, NY, PA, TN, TX |
| Quantity | 612 bottles |
| Reason classes | foreign material, labeling |
| UPC / GTIN / UDI-DI | 00041260351211 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0803-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.