Drug recall
Glucosamine 750 mg 120 ct, Capsule, Dosage: 1 2 capsules, 750 mg ea., three times daily with meals
FDA recall event 71664 · Class II · Novacare, LLC
Key facts
| Event ID | 71664 |
|---|---|
| Recall numbers | F-2946-2015 |
| Recalling firm | Novacare, LLC |
| Product type | Food |
| Products | Glucosamine 750 mg 120 ct, Capsule, Dosage: 1 2 capsules, 750 mg ea., three times daily with meals |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling. |
| Initiation date | May 27, 2015 |
| Report date | Aug 19, 2015 |
| Termination date | Mar 27, 2017 |
| City | Murray |
| State | UT |
| Country | United States |
| FEI number | 1000220648 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: