FDA Recalls Aruba Aloe Hand Sanitizer for Methanol Contamination
FDA is recalling 5,299 bottles of Aruba Aloe Hand Sanitizer Gel nationwide due to methanol contamination in the ethanol ingredient. Consumers should stop using the product immediately.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: FDA Class I classification requires a minimum severity score of 4. Methanol contamination in a hand sanitizer presents a significant health risk through dermal and potential ingestion exposure, though no illnesses are reported in the source text.
Plain-English summary
Aruba Aloe Balm N.V. is recalling Aruba Aloe Hand Sanitizer Gel, 80% Alcohol, 12 fl oz (355 mL) bottles. The recall is nationwide in the United States and affects approximately 5,299 bottles manufactured in Aruba.
The product was manufactured with ethanol that contains methanol contamination. Methanol is a toxic substance that can be absorbed through the skin.
The affected product bears the following lot numbers and expiration dates: Lot #25160 (Exp 4/16/2024), Lot #25344 (Exp 5/20/2024), Lot #25580 (Exp 6/15/2024), Lot #25828 (Exp 7/28/2024), Lot #26057 (Exp 8/25/2024), Lot #26195 (Exp 9/18/2024), Lot #26471 (Exp 11/25/2024), Lot #26754 (Exp 1/20/2025), Lot #26821 (Exp 2/2/2025), Lot #27005 (Exp 3/11/2025), Lot #27518 (Exp 6/22/2025), Lot #27927 (Exp 8/26/2025), Lot #28176 (Exp 10/22/2025), and Lot #28392 (Exp 12/31/2025). The product UPC is 0 82252 03300 5.
Consumers who have this product should stop using it immediately and contact their healthcare provider or poison control if they have experienced any symptoms after use.
The recalled product
- Product
- 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
- Manufacturer
- Aruba Aloe Balm N.V.
- Category
- Drug — Hand Sanitizer
- Hazard
- methanol-contamination
- chemical-contamination
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 (20)
- Lot #: 25160
- Exp 4/16/2024
- 25344
- Exp 5/20/2024
- 25580
- Exp 6/15/2024
- 25828
- Exp 7/28/2024
- 26057
- Exp 8/25/2024
- 26195
- Exp 9/18/2024
- 26471
- Exp 11/25/2024
- 26754
- Exp 1/20/2025
- 26821
- Exp 2/2/2025
- 27005
- Exp 3/11/2025
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- SevereErythromycin Tablets Recalled for Impurity Above Acceptable Limits
FDA (Drugs) · 2026-05-27
- ModerateVitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid
FDA (Drugs) · 2026-05-27
- SevereAtomoxetine Capsules Recalled Due to Labeling Mix-Up Error
FDA (Drugs) · 2026-05-27
- ModeratePrimidone Tablets Recalled Due to API Cross-Contamination
FDA (Drugs) · 2026-05-27