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Author Topic: RECALL: CERTAIN HAND SANITIZERS  (Read 2383 times)
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Mere
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« on: June 09, 2009, 11:59:29 AM »

http://www.foxnews.com/story/0,2933,525520,00.html

CLICK LINK TO ACCESS ENTIRE ARTICLE

FDA Warns of 'High Levels' of Disease-Causing Bacteria Found in Certain Hand Sanitizers
Tuesday, June 09, 2009 
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2NJSons_Mom
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« Reply #1 on: June 10, 2009, 09:32:39 AM »

http://www.foxnews.com/story/0,2933,525520,00.html

CLICK LINK TO ACCESS ENTIRE ARTICLE

FDA Warns of 'High Levels' of Disease-Causing Bacteria Found in Certain Hand Sanitizers
Tuesday, June 09, 2009 


How bizarre is this?   Thanks, Mere. 
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Mere
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« Reply #2 on: June 10, 2009, 01:55:26 PM »

ALL HAND SANITIZERS NOT INVOLVED....PLEASE READ ARTICLE....INVOLVES CLARCON ONLY

http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm164845.htm

Consumers Warned Not to Use Clarcon Skin Products 
 
Risk of bacterial contamination has led the Food and Drug Administration (FDA) to warn consumers to not use any products made by Clarcon Biological Chemistry Laboratory Inc.

The Roy, Utah, firm voluntarily recalled some skin sanitizers and skin protectants sold under a variety of brand names after a recent FDA inspection found that the products contained high levels of disease-causing bacteria.



What products are consumers being warned not to use?

Consumers should not use any Clarcon products. Examples of these products include

• 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



What should consumers do with these products if the have them?

Stop using them immediately and throw them away in household refuse.



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.



How can consumers report adverse events resulting from these products?

Health care professionals and consumers may report serious adverse events (side effects) or product quality problems with the use of this product to the FDA's MedWatch Adverse Event Reporting program.



This article appears on FDA's Consumer Updates page, which features the latest on all FDA-regulated products.

     
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For More Information

FDA Warns Consumers Not to Use Skin Products Made by Clarcon Due to Bacterial Contamination Risk 
MedWatch: The FDA Safety Information and Adverse Event Reporting Program 
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