Nature's Truth Calcium Plus D3 Softgels Recalled for Temperature Excursions
Cardinal Health is recalling Nature's Truth Absorbable Calcium 1200 mg plus D3 5000 IU softgels due to intermittent temperature excursions during storage.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a CGMP deviation (temperature excursion) without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Cardinal Health Inc. is recalling Nature's Truth Absorbable Calcium 1200 mg plus D3 5000 IU 120 Softgels. The recall involves 8 bottles distributed in Florida, Georgia, and South Carolina. All lots distributed between February 23, 2021, and March 10, 2021, are affected.
The recall was initiated due to Current Good Manufacturing Practice (CGMP) deviations, specifically intermittent exposure to temperature excursions during storage. The U.S. Food and Drug Administration has classified this as a Class II recall.
Consumers who have purchased these products should stop using them and contact Cardinal Health Inc. for further instructions or a refund.
The recalled product
- Product
- Nature's Truth Absorbable Calcium 1200 mg plus D3 5000 IU 120 Softgels Dietary Supplements Carefully Designed and Distributed by Nature's Truth LLC. Ronkonkoma, NY 11779, UPC 840093100672
- Manufacturer
- Cardinal Health Inc.
- Category
- Drug — Dietary Supplement
- Affected units
- 8
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All Lots distributed 02/23/2021 through 03/10/2021.
Distribution
Part of a larger recall action
This product is one of 198 recalled by Cardinal Health Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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