CLASS II Drug recall · Reported 15 Feb 2023 · FDA Enforcement Report

Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v recalled

Urban Electric Power is recalling Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v, distributed nationwide in the US. The recall was initiated on 17 Jan 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots within expiry
Quantity recalled609 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0264-2023
FDA event ID
91576
Recalling firm
Urban Electric Power, Pearl River, NY
Classification
Class II
Status
Terminated
Recall initiated
17 Jan 2023
FDA classified
8 Feb 2023
Reported
15 Feb 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Drug class
Hand Sanitizer

Timeline

17 Jan 2023Recall initiated by company
8 Feb 2023Classified by FDA+22 days
15 Feb 2023Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Product as listed by the FDA

Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v, 8 FL OZ (237 ML) bottles.

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Why was it recalled?

CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Which lots are affected?

All lots within expiry

Where was it sold?

Nationwide within the United States

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 91576

More recalls from Urban Electric Power

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