Urgent Recall: FDA Pulls More Acne Products Linked to Cancer-Causing Chemicals – Discover the Complete List!
In recent news, the FDA has issued a recall for several acne products due to contamination with benzene, a chemical associated with cancer risks. While the detection of elevated benzene levels is concerning, the FDA assures consumers that the chances of developing cancer from these products remain very low. However, it is essential to stay informed and periodically check your skincare items for expirations.
On Tuesday, six more acne products were voluntarily recalled after the Food and Drug Administration conducted tests that found benzene contamination. The affected brands include Walgreens, Proactiv, SLMD, and Zapzyt, all of which have been removed from the shelves following thorough evaluations of 95 different acne products containing benzoyl peroxide.
This expanded recall follows L’Oreal’s earlier decision to recall its La Roche-Posay Effaclar Duo Dual Action Acne Treatment due to the same contamination issue. The proactive measures taken reflect the industry’s commitment to consumer safety.
Which Acne Products Have Been Recalled?
The FDA has identified the following acne treatment products that have been voluntarily recalled:
- La Roche-Posay Effaclar Duo Dual Action Acne Treatment
Lot Number(s): MYX46W
Expiration Date: April 2025 - Walgreens Acne Control Cleanser
Lot Number(s): 23 09328
Expiration Date: September 2025 - Proactiv Emergency Blemish Relief Cream Benzoyl Peroxide 5%
Lot Number(s): V3305A; V3304A
Expiration Date: October 2025 - Proactiv Skin Smoothing Exfoliator
Lot Number(s): V4204A
Expiration Date: July 2025 - SLMD Benzoyl Peroxide Acne Lotion
Lot Number(s): 2430600
Expiration Date: March 2025 - Walgreens Tinted Acne Treatment Cream
Lot Number(s): 49707430
Expiration Date: March 2026
Additionally, it’s worth noting that the Zapzyt Acne Treatment Gel was also voluntarily recalled by its manufacturer due to elevated benzene levels found during testing.
Why Were These Acne Products Recalled?
The products in question were recalled due to the presence of benzene, a known carcinogen. The FDA explains that benzene can occur naturally and also be generated through various human activities. In some cases, benzoyl peroxide, a common ingredient in acne treatments, can degrade into benzene under certain conditions.
Following troubling results from third-party tests raising concerns over high benzene levels, the FDA initiated its own testing of 95 acne products. The results revealed that the six mentioned products had elevated benzene levels, although more than 90% of the tested products showed undetectable or very low levels of this chemical.
The FDA has committed to releasing comprehensive results from their testing in the coming months. Importantly, even though elevated benzene levels were detected, the agency has reassured the public that “the risk of a person developing cancer because of exposure to benzene found in these products is very low.”
What to Do if You Have These Acne Products at Home
The FDA has conducted these voluntary recalls on a retail level, meaning that specific products are being taken off the shelves and are no longer available online or in stores. Currently, there are no mandatory steps that consumers need to take regarding products they may already have at home. However, the FDA advises:
- Check any acne products you own for expiration dates.
- If a product has expired, consider discarding it.
While this situation unfolds, it’s crucial for consumers to remain aware of their products and prioritize their health. Regularly reviewing skincare items can help ensure that you are using safe and effective treatments for acne.
For further updates and safety information, stay tuned for more announcements from the FDA and other health authorities.
