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.
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 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.
See all 22 products in this recall →Related recalls
Same manufacturer · Sprayology
See all →- ModerateSprayology Recalls Body Balance Homeopathic Oral Spray Due to CGMP Deviations
FDA (Drugs) · 2018-11-07
- ModerateSprayology Recalls PMS Support Homeopathic Oral Spray Due to CGMP Deviations
FDA (Drugs) · 2018-11-07
- ModerateSprayology Recalls Diet Power Homeopathic Oral Spray Due to CGMP Deviations
FDA (Drugs) · 2018-11-07
- SevereSprayology Recalls Snore Soother Homeopathic Oral Spray Due to CGMP Deviations
FDA (Drugs) · 2018-11-07
- HighSprayology Recalls Man Power Homeopathic Oral Spray Due to CGMP Deviations
FDA (Drugs) · 2018-11-07
Same hazard · microbial contamination
See all →- HighSV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination
FDA (Drugs) · 2026-10-07
- HighSV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination
FDA (Drugs) · 2026-10-07
- SevereMedline Ultrasound Breast Pack Recalled for Potential Sterility Breach
FDA (Devices) · 2026-09-09
- HighMedline Convenience Kits Recalled for Potential Sterility Breach
FDA (Devices) · 2026-09-09
- CriticalOptimal Balance Pharmacy Recalls Contaminated Glutathione Injection Vials
FDA (Drugs) · 2026-09-09
Similar recalls
- ModerateDrug Recall: SnoreStop Naso Spray Bulk for cGMP Manufacturing Deviations
FDA (Drugs) · 2023-07-05
- HighFDA Recalls StellaLife VEGA Oral Care Spray for Manufacturing Practice Violations
FDA (Drugs) · 2023-07-05
- ModerateDrug Recall: Purely Soothing MSM Nasal Spray due to manufacturing deviations
FDA (Drugs) · 2023-03-15
- ModerateOxymetazoline Nasal Spray Recalled Due to Manufacturing Process Deviation
FDA (Drugs) · 2024-01-10
- ModerateDrug Oral Care Spray Recalled for Manufacturing Practice Deviations
FDA (Drugs) · 2023-07-05
- ModerateBeaumont Bio-Med Recalls Diarrhea Response Homeopathic Formula Due to CGMP Deviations
FDA (Drugs) · 2018-09-26