Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Ongoing Initiated Mar 23, 2024 (3 years ago)

Aruba Aloe Hand Sanitizer Gel

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Chemical Contamination: Product manufactured with ethanol API that contains methanol

Cause type: Chemical / undeclared

A chemical that should not be there - benzene, methanol, lead - or an undeclared prescription drug hidden in a supplement. The label gives no warning: you may be taking a toxic solvent, a heavy metal, or a drug such as sildenafil that interacts with your other medicines. All chemical / undeclared recalls.

What was recalled

Aruba Aloe Hand Sanitizer Gel, 80% Alcohol, 12 fl oz (355 mL) plastic bottle, Manufactured in Aruba by Aruba Aloe Balm Inc., Pitastraat 115, Aruba, Dutch Caribbean. UPC 0 82252 03300 5

Drug: Alcohol

Recalling firm
Aruba Aloe Balm N.V.
Origin
N/A, Aruba
Initiated by
Voluntary: Firm initiated
Company announcement
Apr 5, 2024 · FDA notice with lot numbers
FDA recall number
D-0460-2024 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week.

Other Alcohol recalls

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Other recalls by Aruba Aloe Balm N.V.

All 2024 recalls
Class I · High risk

Alcoholada Gel

Chemical Contamination: Product manufactured with ethanol API that contains methanol

Ongoing Chemical / undeclared Aruba Aloe Balm N.V. D-0459-2024