Ohm Sanitizer Spray Recalled Due to Chemical Contamination
Urban Electric Power is recalling Ohm Sanitizer Spray nationwide because FDA analysis found the product contains acetaldehyde and acetal above specification limits.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA classified this as Class II. Although Class II recalls can indicate serious health consequences, no illnesses or injuries have been reported in connection with this product. The documented hazard is chemical contamination above specification limits, representing a manufacturing deviation. Per the rubric, when no illnesses are reported and the hazard is theoretical in impact, the score is at most 3.
Plain-English summary
Urban Electric Power is recalling all lots of Ohm Sanitizer Spray (80% ethyl alcohol, 8 FL OZ bottles) distributed nationwide in the United States. The recall was initiated due to Current Good Manufacturing Practice (CGMP) deviations identified by FDA analysis.
FDA testing found that the product contains acetaldehyde and acetal above specification limits. These chemicals are present in excess of acceptable manufacturing standards.
Consumers who have purchased Ohm Sanitizer Spray should stop using the product immediately. For further information about this recall or instructions regarding product return or disposal, consumers may contact Urban Electric Power or the FDA.
The recalled product
- Product
- Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v, 8 FL OZ (237 ML) bottles.
- Manufacturer
- Urban Electric Power
- Category
- Drug — Sanitizer
- Affected units
- 609
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 2 recalled by Urban Electric Power 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 2 products in this recall →Related recalls
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