MPRX Recalls Magic Bullet Supplement Due to Expired Components
MPRX, Inc. is recalling Magic Bullet Supplement bottles compounded with expired components and incorrect labeling. The recall affects products distributed in Texas.
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 involves labeling errors and the use of expired components, which aligns with the rubric for moderate severity involving minor labeling errors or low-risk contamination.
Plain-English summary
MPRX, Inc. dba Medical Park Pharmacy is recalling one bottle of Magic Bullet Supplement. The recall is due to labeling errors, specifically incorrect or missing lot and expiration dates, and the use of expired components in the compounding process.
The affected product is identified by Lot 61048:99 with a use-by date of 02/08/2020. The recall is limited to products distributed in Texas.
Consumers who have this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Magic Bullet Supplement
- Manufacturer
- MPRX, Inc. dba Medical Park Pharmacy
- Category
- Drug — Compounded Supplement
- Affected units
- 1
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)
- Lot: 61048:99 Use by: 02/08/2020
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 18 recalled by MPRX, Inc. dba Medical Park Pharmacy 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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