Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser on September 12, 2025. The recall follows the discovery of elevated benzene levels in the product. This contamination poses a high health risk to consumers in California and Georgia.
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Consumers and healthcare providers should stop using this product immediately. Contact Private Label Skin Care Inc. or your healthcare provider for guidance. Notification method: Letter
The recalled product is Skin MD Body Acne Cleanser, containing 10% benzoyl peroxide, in 7 oz (201 g) bottles. It is associated with Lot # 58170A and 58172A, with an expiration date of September 2025. The product was distributed in California and Georgia.
The recall was initiated due to the detection of elevated levels of benzene, a harmful chemical. Benzene exposure can lead to serious health issues, making this a significant safety concern.
No specific incidents or injuries have been reported related to this recall. However, the presence of benzene poses a high risk to users.
Consumers should stop using the product immediately. Contact Private Label Skin Care Inc. or consult your healthcare provider for further guidance.
For more information, visit the FDA website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0664-2025 or reach out to Private Label Skin Care Inc.
Abiomed issued a recall for 10,153 Automated Impella Controllers on October 1, 2025. The devices face potential cybersecurity vulnerabilities related to their operating system. Healthcare providers and patients should stop using these devices immediately.
Acuity Specialty Products recalled its Wyandotte Sanifect E3 hand sanitizer on September 29, 2025. The recall affects multiple package configurations due to potential methanol contamination. Consumers should stop using the product immediately and contact the company for guidance.
AFCO recalled hand sanitizer on September 29, 2025, due to a risk of methanol contamination. The company failed to conduct required testing on incoming alcohol components. Consumers should stop using the product immediately.