Kroger Specialty Pharmacy Recalls Boost VHC Oral Liquid Due to Processing Controls
Kroger Specialty Pharmacy is recalling Boost VHC Oral Liquid due to a lack of processing controls. The product was distributed in five states.
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, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Kroger Specialty Pharmacy, Inc. is recalling Boost VHC Oral Liquid VAN #27 (NDC 43900-0182-15), a 27-day supply, due to a lack of processing controls. The recall affects all lots remaining within expiry that were dispensed between December 1, 2017, and February 12, 2018.
The product was distributed in Mississippi, Louisiana, Arkansas, Illinois, and Florida. The source text does not specify the number of units affected or report any illnesses or injuries associated with the product.
Consumers who have this product should stop using it and contact their healthcare provider or the pharmacy for further instructions.
The recalled product
- Product
- Boost VHC Oral Liquid VAN #27 NDC 43900-0182-15 27 days supply
- Manufacturer
- Kroger Specialty Pharmacy, Inc.
- Category
- Drug — Oral Liquid
- Hazard
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 remaining within expiry dispensed 12/01/2017 through 02/12/2018
Distribution
Part of a larger recall action
This product is one of 67 recalled by Kroger Specialty Pharmacy, 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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