Laksell Gamma Knife Perfexion
Reported: November 5, 2014 Initiated: October 6, 2014 #Z-0152-2015
Product Description
Laksell Gamma Knife Perfexion
Reason for Recall
Elekta has become aware that the latches may be locked before they have been fully turned resulting in a poorly locked frame.
Details
- Recalling Firm
- Elekta, Inc.
- Units Affected
- 181
- Distribution
- Worldwide Distribution - USA (nationwide) including the states of AK, AZ, AR, CA, CO, CT, FL, GA, HI, IL, KY, LA, MA, MI, MN, MS, MO, MT, NJ, NM, NY, NC, OH, OR, PA, RI, SC, TX, TN, UT, VA, WA and WV, and the countries of Australia, Austria, Belgium, Brazil, Canada, China, Colombia, Czech Republic, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Italy, Japan, Mexico, Morocco, Netherland, Norway, Poland, Portugal, Russia, Saudi Arabia, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey and United Kingdom.
- Location
- Atlanta, GA
Frequently Asked Questions
What product was recalled? ▼
Laksell Gamma Knife Perfexion. Recalled by Elekta, Inc.. Units affected: 181.
Why was this product recalled? ▼
Elekta has become aware that the latches may be locked before they have been fully turned resulting in a poorly locked frame.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 5, 2014. Severity: Moderate. Recall number: Z-0152-2015.
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