FDA Issues Urgent Recall for Hand Sanitizer and Aloe Gel Amid Health Risk Warnings
FDA Issues Urgent Recall for Hand Sanitizer and Aloe Gel Amid Health Risk Warnings
Highlights
- FDA issues an urgent recall for Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel due to methanol contamination, posing serious health risks to consumers.
- Methanol exposure can lead to nausea, vomiting, blurred vision, coma, seizures, permanent blindness, and death, prompting immediate cessation of product use.
- Over 600 potentially dangerous hand sanitizers have been identified during the pandemic, emphasising the need for stringent safety standards and regulatory oversight.
- Aruba Aloe Balm N.V. offers guidance to impacted consumers and provides discount coupons for future purchases, prioritising consumer safety amidst the recall.
Consumers are urged to take heed as federal health officials issue a stark warning regarding the potential dangers lurking in certain hand sanitizer and aloe gel products.
The Food and Drug Administration (FDA) has initiated a recall of 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel due to the presence of methanol, a hazardous substance that poses severe health risks.
Methanol, a toxic compound commonly found in industrial settings, has been identified in these recalled products, raising concerns over potential adverse effects on consumers.
The FDA underscores the gravity of the situation, cautioning that exposure to substantial levels of methanol can lead to a range of serious health complications, including nausea, vomiting, headache, blurred vision, coma, seizures, permanent blindness, and even death. This alarming revelation has prompted urgent action to safeguard public health.
The affected products, manufactured by Aruba Aloe Balm N.V., are identifiable by their packaging and labelling.
The Aruba Aloe Hand Sanitizer Gel Alcohol 80% is packaged in 12-ounce dark green plastic bottles adorned with white labels bearing the inscription “ARUBA ALOE Hand Sanitizer Gel Alcohol 80% Made in Aruba, World’s Finest Aloe.”
Meanwhile, according to FOX Business, the Aruba Aloe Alcoholada Gel, designed for temporary relief of pain and itching from minor burns, sunburn, insect bites, or skin irritations, is available in two sizes: 2.2 fl oz and 8.5 fl oz plastic bottles, both featuring transparent packaging and labels indicating “Alcoholada Gel Pain Relieving Gel 0.5% Lidocaine Hydrochloride.”
This urgent recall underscores the critical importance of meticulous product evaluation and adherence to stringent safety standards, especially in light of the ongoing pandemic.
The FDA’s vigilance in monitoring hand sanitizer formulations has led to the identification of over 600 potentially hazardous products, highlighting the prevalence of unapproved substances like methanol in certain formulations.
While ethyl alcohol remains the preferred active ingredient for hand sanitizers, the infiltration of methanol poses a significant risk to consumer safety.
Furthermore, the FDA emphasises the heightened vulnerability of certain demographics, particularly young children and adolescents, to methanol poisoning.
Accidental ingestion or misuse of these products can exacerbate the risk of adverse health effects, underscoring the need for immediate cessation of use and proper disposal.
Despite the absence of reported adverse events associated with these products, Aruba Aloe Balm N.V. has taken proactive measures to address the issue swiftly.
The affected lots were distributed between May 1, 2021, and October 7, 2023, and were primarily sold online through the company’s website.
In response to the recall, the company has initiated communication with impacted customers, offering vital guidance and a discount coupon for future purchases. This proactive approach aims to mitigate potential harm and reinforce consumer confidence in product safety.
As consumers navigate the marketplace for essential hygiene products, heightened vigilance and awareness are paramount to safeguarding personal health and well-being.
The FDA’s swift action serves as a reminder of the critical role regulatory agencies play in ensuring product safety and protecting public health in the face of emerging threats.
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