Medical Park Pharmacy Recalls DHEA/Pregnenol One Capsules Due to Labeling Errors
MPRX, Inc. dba Medical Park Pharmacy is recalling DHEA/Pregnenol One 10.25 MG Capsules because they were compounded using expired components and have incorrect or missing lot and expiration dates.
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 due to labeling errors and the use of expired components, which fits the rubric for moderate severity involving minor labeling errors or low-risk contamination without reported serious injuries.
Plain-English summary
MPRX, Inc. dba Medical Park Pharmacy is recalling DHEA/Pregnenol One 10.25 MG Capsules. The recall is due to labeling issues where the products have incorrect or missing lot and/or expiration dates. Additionally, the source text states that the products were compounded using expired components.
The affected product is identified as Lot L61406:42 with a use-by date of 05/06/2020. The distribution pattern is listed as TX, indicating the products were distributed in Texas. The quantity is 1 bottle.
Consumers who have this product should stop using it and contact the recalling firm or their healthcare provider for further instructions. The FDA has classified this recall as Class II, which means there is a reasonable probability that the use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences.
The recalled product
- Product
- DHEA/Pregnenol One 10.25 MG Cap
- Manufacturer
- MPRX, Inc. dba Medical Park Pharmacy
- Category
- Drug — Compounded Medication
- 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: L61406:42 Use by: 05/06/2020
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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