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Outpatient Surgery E-Weekly

Unlicensed Cosmetic Surgery Hospitalizes 6 in N.J.

New Jersey medical authorities are investigating the incidence of and issuing alerts on unlicensed cosmetic surgery providers after 6 women suffered...

Rotator Cuff Repair Restores Strength, Not Function

Rotator cuff surgery may restore a patient's normal shoulder strength, but mobility issues persist in the repaired joint, according to researchers a...

Do Patients Expect Too Much From Joint Replacement?

Even with a thorough pre-op education program, more than two-thirds of joint replacement patients don't share the expectations that their surgeons d...

Home > News > October, 2009
Care-Tech Laboratories Suspends Operations Amid FDA Probe
St. Louis-based company agrees to stop making, selling and distributing unnapproved antimicrobial products.

Care-Tech Laboratories, makers of Techni-Care pre-operative prep solutions and surgical scrub and several other over-the-counter antimicrobial drugs used to treat and prevent infection, has signed a consent decree, agreeing to stop the illegal manufacture, marketing and distribution of its products, says the U.S. Food and Drug Administration.

FDA inspectors found that Care-Tech violated numerous provisions of the FDA's current good manufacturing practice (cGMP) regulations that direct how antimicrobial drugs are made. Additionally, the products do not conform to any applicable regulations for OTC drug products and have not undergone an FDA review, and therefore are considered unapproved drug products.

Under the terms of the consent decree, Care-Tech may not resume manufacturing and distribution of the drugs until it corrects these and other violations. Neither FDA nor Care-Tech is aware of any reports of injury or illness related to the use of these products, and FDA has not issued a product recall. "The company is committed to ensuring that each of its products reflects the highest standards of safety and purity," says John C. Brereton, the president of Care-Tech.

Dan O'Connor

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