Aruba Aloe: Hand Sanitizer Gel and Alcoholada Gel — FDA announcement Apr 5, 2024

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Apr 5, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Hand Sanitizer Gel and Alcoholada Gel
Reason
Product contains methanol
Classification
Not supplied
Recalling firm
Aruba Aloe Balm N.V.
Quantity
Not supplied
Agency-reported status
Company recall announcement
Source record identifier
1aa416547aabc92c

Open the official record

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityAruba Aloe Hand Sanitizer Gel is used as a sanitizer to help reduce bacteria that potentially can cause disease and is packaged in 12 fl oz (355 mL) dark green plastic bottles with white label reading in part “ARUBA ALOE Hand Sanitizer GEL 80% Alcohol Made in Aruba World’s Finest Aloe”, with barcode 0 82252 03300 5. Lot numbers being recalled are listed in the below table.; Aruba Aloe Alcoholada Gel is used for temporary relief of pain and itching associated with minor burns, sunburn, insect bites, or minor skin irritations and is packaged in two sizes: 2.2 fl oz (65 mL) plastic bottles with barcode 0 82252 34030 1 and 8.5 fl oz (251 mL) plastic bottles with barcode 0 82252 03120 9. The plastic bottles are transparent with a label reading in part “Alcoholada Gel Pain Relieving Gel 0.5% Lidocaine Hydrochloride”. Lot numbers being recalled are listed in the below table.; Lot Number | Expiration date; 25344 | 5/20/2024; 25828 | 7/28/2024; 26057 | 8/25/2024; 26471 | 11/25/2024; 26754 | 1/20/2025; 26821 | 2/2/2025; 27518 | 6/22/2025; 28392 | 12/31/2025; 24759 | 3/4/2024; 25160 | 4/16/2024; 25580 | 6/15/2024; 26195 | 9/18/2024; 27005 | 3/11/2025; 27927 | 8/26/2025; 28176 | 10/22/2025; Lot Number | 8.5 oz | 2.2 oz | Expiration date; 25253 | X | X | 5/1/2024; 25976 | X | X | 8/11/2024; 26150 | X | X | 9/11/2024; 26473 | X | | 11/25/2024; 26553 | X | X | 12/11/2024; 26696 | | X | 1/8/2025; 27318 | X | X | 5/10/2025; 27481 | X | X | 6/15/2025; 27660 | X | X | 7/15/2025; 27839 | X | X | 8/5/2025; 28121 | X | | 10/7/2025; 28152 | X | | 10/18/2025; 28281 | | X | 11/30/2025; 28355 | X | X | 12/17/2025; 28761 | X | X | 2/22/2026; 29088 | X | X | 4/1/2026; 29510 | X | | 5/11/2026; 29558 | X | | 5/13/2026; 29728 | X | X | 6/3/2026; 30086 | | X | 7/26/2026; 30339 | X | X | 9/13/2026; 30563 | X | X | 10/27/2026

Match all identifying details in the current notice. A brand name alone is not enough.

Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

FDA company announcement, table 1
Lot Number Expiration date
25344 5/20/2024
25828 7/28/2024
26057 8/25/2024
26471 11/25/2024
26754 1/20/2025
26821 2/2/2025
27518 6/22/2025
28392 12/31/2025
24759 3/4/2024
25160 4/16/2024
25580 6/15/2024
26195 9/18/2024
27005 3/11/2025
27927 8/26/2025
28176 10/22/2025
FDA company announcement, table 2
Lot Number 8.5 oz 2.2 oz Expiration date
25253 X X 5/1/2024
25976 X X 8/11/2024
26150 X X 9/11/2024
26473 X 11/25/2024
26553 X X 12/11/2024
26696 X 1/8/2025
27318 X X 5/10/2025
27481 X X 6/15/2025
27660 X X 7/15/2025
27839 X X 8/5/2025
28121 X 10/7/2025
28152 X 10/18/2025
28281 X 11/30/2025
28355 X X 12/17/2025
28761 X X 2/22/2026
29088 X X 4/1/2026
29510 X 5/11/2026
29558 X 5/13/2026
29728 X X 6/3/2026
30086 X 7/26/2026
30339 X X 9/13/2026
30563 X X 10/27/2026

Announcement retrieved Oct 1, 2026. Official announcement.

Distribution

Not supplied

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Fda listing date
Apr 5, 2024
Company announcement date
Apr 5, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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