Sprayology Recalls MenoPower Homeopathic Oral Spray Due to CGMP Deviations
Sprayology is recalling MenoPower Homeopathic Oral Spray because it was manufactured under conditions that could result in possible microbial contamination.
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 a theoretical risk of microbial contamination without reported illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Sprayology is recalling 2,301 bottles of MenoPower Homeopathic Oral Spray, 1.38 fl. oz (41ml). The product is identified by NDC 61096-0014-1 and Tester NDC 61096-1014. All lots within expiry are affected.
The recall was initiated due to Current Good Manufacturing Practice (CGMP) deviations. The product was manufactured by a contract manufacturer under conditions that could result in possible microbial contamination.
The product was distributed nationwide in the USA. Consumers should stop using the product and contact Sprayology for further instructions.
The recalled product
- Product
- MenoPower, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0014-1 and Tester NDC 61096-1014
- Manufacturer
- Sprayology
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 2,301
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 within expiry
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 22 recalled by Sprayology 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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