Glucosamine 750 mg recalled over undeclared allergens
- Recall date
- May 27, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Novacare, LLC recalls Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
- Recall number
- F-2946-2015
- FDA classification
- Class II
- Brand / firm
- Novacare, LLC
- Sold / distributed
- Nationwide. No foreign or VA/govt/military consignees.
Why it was recalled
TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
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