Glucosamine 750 mg 120 ct — Class II food recall F-2946-2015
Terminated recall by Novacare, LLC, reported 2015-08-19, distributed nationwide. TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.
| Recall number | F-2946-2015 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Novacare, LLC, Murray, UT, United States |
| Recall initiated | 2015-05-27 |
| Classified | 2015-08-11 |
| Reported by FDA | 2015-08-19 |
| Terminated | 2017-03-27 |
| Distributed | Nationwide (US) |
| Quantity | 961 bottles |
| Reason classes | undeclared allergen, labeling |
| Lot numbers | 2032006, 2061401, 2071918.2, 4102801 |
Product
Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
Reason for recall
TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.
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-2946-2015. 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.