Cardinal Health Recalls Therapeutic M 130 Tablets Due to Temperature Excursions
Cardinal Health is recalling 55 bottles of Therapeutic M 130 tablets due to intermittent temperature excursions during storage.
What this means for you
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, which typically involves a situation that might cause temporary or medically reversible adverse health consequences. The hazard is a CGMP deviation (temperature excursion) without reported illnesses, fitting the Moderate criteria for low-risk contamination or voluntary precautionary recalls.
Plain-English summary
Cardinal Health Inc. is recalling 55 bottles of Therapeutic M 130 tablets (NDC/UPC 740985223680). The recall was initiated because of Current Good Manufacturing Practice (CGMP) deviations involving intermittent exposure to temperature excursions during storage.
The affected lots were distributed between February 23, 2021, and March 10, 2021. The products were distributed in Florida, Georgia, and South Carolina.
Consumers who have this product should stop using it and contact Cardinal Health Inc. for further instructions or a refund.
The recalled product
- Product
- THERAPEUTIC M 130; NDC/UPC 740985223680; OTC; TABLETS
- Manufacturer
- Cardinal Health Inc.
- Affected units
- 55
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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