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- Aruba Aloe Balm N.V. Issues Voluntary Nationwide Recall of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel Due to Presence of Methanol When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company.
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May 28, 2024 · The U.S. Food and Drug Administration (FDA) inspected your drug manufacturing facility, Aruba Aloe Balm N.V., FEI 3004117460, at Pitastraat 115, Oranjestad, from November 13 to 16, 2023. This...
Apr 5, 2024 · When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the...
Jun 27, 2017 · In order to hold on to its certifications, Aruba Aloe must undergo an annual inspection by ISO auditors, which it passed this year with flying colors, thereby holding on firmly to both of these prestigious certifications.
The Food and Drug Administration announced a recall of 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel, both of which pose a risk of methanol exposure.
Apr 8, 2024 · The two products, Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel, were found to contain methanol, which is toxic to the skin and poisonous if ingested.
- Chloe Mayer
- 1 min
ISSUE: Aruba Aloe Balm N.V. is recalling 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel because the products have been found to contain alcohol denatured with methanol.
Apr 9, 2024 · FDA. The company said there have been no reported adverse events related to these products thus far, but methanol exposure can lead to severe consequences, including nausea, vomiting, headache, blurred vision, coma, seizures, permanent blindness, and even death.