MasterPharm Recalls Estriol 6 mg Capsules Due to Processing Control Deficiencies
MasterPharm LLC is recalling Estriol 6 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
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, injuries, or hospitalizations, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
MasterPharm LLC is voluntarily recalling Estriol 6 mg capsules, 90 capsules per bottle, distributed nationwide in the United States. The recall is being conducted because of a lack of processing controls, which means there is a lack of assurance that the product conforms to its specifications.
The affected product is identified by the code 01-23-2020:03@5 and has a best-use date of 7/21/2020. The recall is classified as Class II by the U.S. Food and Drug Administration.
Consumers who have purchased this product should stop using it and contact MasterPharm LLC at (866) 630-5600 for further instructions or a refund.
The recalled product
- Product
- Estriol 6 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
- Manufacturer
- MasterPharm LLC
- Category
- Drug — Prescription Drug
- Hazard
- Affected units
- 90
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 (2)
- 01-23-2020:03@5
- BUD 7/21/2020
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 26 recalled by MasterPharm LLC 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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