Progesterone 200 mg Troche Recalled for Expired Components and Labeling Errors
MPRX, Inc. is recalling Progesterone 200 mg Troche due to incorrect labeling and the use of expired components in compounding.
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 without reported injuries.
Plain-English summary
MPRX, Inc. dba Medical Park Pharmacy is recalling one bottle of Progesterone 200 mg Troche. The recall is due to labeling errors, specifically incorrect or missing lot and expiration dates, and because the products were compounded using expired components.
The affected product is identified by Lot 61242:26 with a use-by date of 02/28/2020. The recall is limited to distribution in Texas (TX).
Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for instructions on disposal or replacement.
The recalled product
- Product
- Progesterone 200 mg Troche
- 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: 61242:26 Use by: 02/28/2020
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.
See all 18 products in this recall →Related recalls
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