FDA recall record

Aruba Aloe Hand Sanitizer Gel, 80% Alcohol, 12 fl oz (355 mL) plastic bottle recall — FDA D-0460-2024

Chemical Contamination: Product manufactured with ethanol API that contains methanol

Class Iclassification
D-0460-2024official record ID
May 1, 2024report date

Recall record at a glance

Official recordD-0460-2024
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmAruba Aloe Balm N.V.
Report dateMay 1, 2024
Recall initiation dateMar 23, 2024
Quantity5299 bottles
LocationOranjestad, N/A, Aruba

Official 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

Why the product was recalled

Chemical Contamination: Product manufactured with ethanol API that contains methanol

Distribution information

Nationwide in the USA

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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