Elekta, Inc. recalls HexaPOD evo RT Couchtop. To support and aid in positioning a patient during radiation therapy.

Recalled May 7, 2014 · FDA recall Z-1514-2014 · Elekta

Hazard

If screws are not properly tightened with a torque wrench they may become loose over time. · FDA Class II

Units

266

Sold at

Worldwide Distribution-USA including DC and the states of AZ, CA, CT, FL, GA, IL, HI, KY, MD, MA, MI, MS, MO, NJ, NY, NH, NC, ND, OH, OK, OR, PA, SC, TX, VA, WA, WI, and WY, and the countries of Algeria, Australia, Austria, Belgium, Brazil, Canada, China, Colombia, Czech Republic, Denmark, Finland, France, Germany, Greece, Hong Kong, India, Israel, Italy, Japan, Kazakhstan, Mexico, Netherlands, New Zealand, Peru, Poland, Portugal, Russia, Saudi Arabia, South Korea, Span, Sweden, Switzerland, Taiwan, Thailand, Turkey, and United Kingdom.

Description

If screws are not properly tightened with a torque wrench they may become loose over time.

Product

HexaPOD evo RT Couchtop. To support and aid in positioning a patient during radiation therapy.

Manufacturer(s)

Elekta, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →