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NEUTROGENA and AVEENO aerosol Sunscreen - recalled due to presence of a carcinogen, USA

2 years ago source www.fda.gov

Recall notice

United States

Company name: Johnson& Johnson
Brand name: Neutrogena, Aveeno
Product recalled: Sunscreen
Reason of the recall: Testing identified low levels of benzene
FDA Recall date: July 14, 2021
Recall details: Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen product lines to the consumer level. Internal testing identified low levels of benzene in some samples of the products. Consumers should stop using the affected products and follow the instructions set forth below.

The only sunscreen products impacted are aerosol products, specifically: NEUTROGENA® Beach Defense® aerosol sunscreen:
- NEUTROGENA® Cool Dry Sport aerosol sunscreen
- NEUTROGENA® Invisible Daily™ defense aerosol sunscreen
- NEUTROGENA® Ultra Sheer® aerosol sunscreen
- AVEENO® Protect + Refresh aerosol sunscreen

Benzene is classified as a human carcinogen, a substance that could potentially cause cancer depending on the level and extent of exposure. Benzene is ubiquitous in the environment. Humans around the world have daily exposures indoors and outdoors from multiple sources. Benzene can be absorbed, to varying degrees, by inhalation, through the skin, and orally. Based on exposure modeling and the Environmental Protection Agency’s (EPA) framework, daily exposure to benzene in these aerosol sunscreen products at the levels detected in our testing would not be expected to cause adverse health consequences. Out of an abundance of caution, we are recalling all lots of these specific aerosol sunscreen products.

While benzene is not an ingredient in any of our sunscreen products, it was detected in some samples of the impacted aerosol sunscreen finished products. We are investigating the cause of this issue, which is limited to certain aerosol sunscreen products. Sunscreen use is critical to public health. Melanoma incidences continue to increase worldwide, and the majority of cases are caused by excessive sun exposure. It is important that people everywhere continue to take appropriate sun protection measures, including the continued use of alternative sunscreen.

The recalled sunscreen products are packaged in aerosol cans. The products were distributed nationwide through a variety of retail channels.

Consumers should stop using these specific products and appropriately discard them.

Check the full recall details on www.fda.gov

Source: FDA

#drugs #recall #johnsonjohnson #us

Recent Interesting Reports

Aruba Aloe Balm N.V. is voluntarily recalling 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel to the consumer level. The products have been found to contain alcohol denatured with methanol. Products were distributed between 5/1/2021 and 10/27/2023 and sold in … See More
the US online only via the Aruba Aloe Balm N.V. website. To date, Aruba Aloe Balm N.V. has not received any reports of adverse events related to these products.

Aruba 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.

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”.

The affected Aruba Aloe Hand Sanitizer GEL product lots (filled in 12, 2.2, and 8.5 fl. oz bottles bottles) can be viewed in the link below.

Aruba Aloe Balm N.V. has notified all customers that bought these products by email and has offered a discount coupon for a next purchase. Consumers that have products which are being recalled should stop using and discard the product.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache blurred vision, coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Aruba Aloe Balm N.V.
Brand name: Aruba Aloe
Product recalled: Hand Sanitizer Gel and Alcoholada Gel
Reason of the recall: Product contains methanol
FDA Recall date: April 05, 2024

Source: www.fda.gov
See Less

#recall #us

F

Scam alert, 192-01 Northern Blvd, Flushing, NY, USA

2 weeks ago reported by user-fmgdv214

I received a Daily Detox from SlimFit Fusion in Flusing NY that I did not order

I received to packages, the last one fro DP 192-01 Northern Blvd. Flusing NY. It was for Daily Detox by Slim Fit Fusion. I also received another package Keto+ACV. Neither were ordered

#ketogummiesscam #unorderedpackage #delivery #newyork #us

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