Nationwide Recall of Personal Care Products Over Sepsis Causing Bacteria Risk
Personal care products distributed nationwide have been recalled after it was discovered that the products may be contaminated with a dangerous, antibiotic-resistant bacterium.
Bacteria Behind the Recall
According to the U.S. Food and Drug Administration, DermaRite Industries, LLC has issued a voluntary recall of specific lots of several over-the-counter personal healthcare products after testing revealed contamination with Burkholderia cepacia complex, a type of bacteria that is commonly found in soil and water, and can cause serious and potentially life-threatening infections.
The affected products were distributed across the United States and Puerto Rico. These products are commonly used for handwashing, relief of minor skin irritations, and personal cleansing, including care for individuals with compromised immune systems.
Who Is Most at Risk
Burkholderia cepacia poses the greatest risk to immunosuppressed individuals, where infection can spread beyond the initial site and potentially lead to sepsis. In healthy users, exposure is more likely to result in localized skin infections, particularly if the skin is broken, according to the Centers for Disease Control and Prevention.
In the United States, people in healthcare settings and those with weakened immune systems or chronic lung diseases, particularly cystic fibrosis, are at highest risk of infection with B. cepacia complex. - CDC
Products Impacted by the Recall
While no adverse events have been reported so far, the company is urging immediate removal of the affected lots from circulation, and consumers should stop using these products immediately:
- DermaKleen antiseptic lotion soap for hands
- DermaSarra external topical analgesic used for skin irritation
- KleenFoam antimicrobial foam soap for hands
- PeriGiene antiseptic cleanser for the perineal area
DermaRite has contacted distributors and customers to quarantine and destroy any impacted products according to facility protocols. Consumers are advised to discontinue use and consult a healthcare provider if they experience any symptoms that may be linked to the recalled items.
What to Do If You Have These Products
Questions regarding the recall can be directed to DermaRite’s Mary Goldberg at 973-569-9000 x104 during business hours or via email at voluntary.action@dermarite.com. Any suspected adverse reactions should be reported to the U.S. Food and Drug Administration’s MedWatch program online or by mail, or by fax.
A complete list of recalled lot numbers is available on the FDA website. Consumers and healthcare facilities are urged to check inventory immediately to ensure contaminated products are not in use, helping reduce the risk of infection in vulnerable populations.
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