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Class I: serious health riskOngoing

Aruba Aloe Hand Sanitizer Gel Recall

Aruba Aloe Hand Sanitizer Gel, 80% Alcohol, 12 fl oz (355 mL) plastic bottle, Manufactu…

Aruba Aloe Balm N.V. · Oranjestad, N/A

Risk level
Class I
Reported by FDA
May 1, 2024
Recall ID
D-0460-2024
Check your lot numberHow we source this data

Summary

Aruba Aloe Balm N.V. recalled Aruba Aloe Hand Sanitizer Gel starting Mar 23, 2024. The FDA classified it as Class I (serious health risk) and published enforcement report D-0460-2024 on May 1, 2024. Reason: Chemical Contamination: Product manufactured with ethanol API that contains methanol. Status: Ongoing.

Why it was recalled

Chemical Contamination: Product manufactured with ethanol API that contains methanol

Product description

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

Lot numbers, UPCs & expiration codes

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; 27518, Exp 6/22/2025; 27927, Exp 8/26/2025; 28176, Exp 10/22/2025; 28392, Exp 12/31/2025.

Where it was sold

Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0460-2024
Classification
Class I
Status
Ongoing
Recall initiated
Mar 23, 2024
FDA report date
May 1, 2024
Quantity
5299 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Aruba Aloe Balm N.V.

Original FDA data

Every field from FDA enforcement report D-0460-2024, exactly as published.

Show all FDA fields
City
Oranjestad
Status
Ongoing
Country
Aruba
Event ID
94335
Address
Pitastraat 115
Code information
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; 27518, Exp 6/22/2025; 27927, Exp 8/26/2025; 28176, Exp 10/22/2025; 28392, Exp 12/31/2025.
Report date
May 1, 2024
Product type
Drugs
Recall number
D-0460-2024
Classification
Class I
Recalling firm
Aruba Aloe Balm N.V.
Product quantity
5299 bottles
Reason for recall
Chemical Contamination: Product manufactured with ethanol API that contains methanol
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Nationwide in the USA
Recall initiation date
Mar 23, 2024
Initial firm notification
E-Mail
Center classification date
Apr 23, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0460-2024, published May 1, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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