Sanitizer Recall
The hand sanitizer recall issued by Clarcon results from tests run on many products they produce showing evidence of unsanitary conditions during manufacture or packaging.
What specific concerns does FDA have about these products?
Analyses of several samples of over-the-counter topical antimicrobial skin sanitizer and hand protectant products revealed high levels of various bacteria, including some associated with unsanitary conditions.
Some of these bacteria can cause opportunistic infections of the skin and underlying tissues. Such infections may need medical or surgical attention, and may result in permanent damage.
FDA finds the inspection results particularly concerning because the products are promoted as antimicrobial agents that claim to treat open wounds, damaged skin, and protect against various infectious diseases.
The inspection uncovered serious deviations from FDA’s requirements.
The Clarcon recall affect these products:
Citrushield Lotion
Dermasentials DermaBarrier
Dermassentials by Clarcon
Antimicrobial Hand Sanitizer
Iron Fist Barrier Hand Treatment
Skin Shield Restaurant
Skin Shield Industrial
Skin Shield Beauty Salon Lotion
Total Skin Care Beauty
Total Skin Care Work
Some of the bacteria found that caused the hand sanitizer recall can cause skin infections. Some of these bacteria can cause opportunistic infections of the skin and underlying tissues and could result in medical or surgical attention as well as permanent damage.
If you have used one of the above products and suffered any type of infection, please contact us.
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