FDA Medical Device Recalls (openFDA)
Elekta, Inc.: Precise Treatment Table Intended as a universal patient treatment support and positioning table for radiation therapy and simulation use.
- Recall number
- Z-1432-2010
- Recalling firm
- Elekta, Inc.
- Product
- Precise Treatment Table Intended as a universal patient treatment support and positioning table for radiation therapy and simulation use.
- Status
- Terminated
- Initiated
- 2007-01-11
- Posted
- 2010-04-23
- Terminated
- 2010-12-28
- Reason
- In some instances, the bolts which are supplied with the table have sheared off, resulting in inability to operate the powered table.
- Root cause
- Other
- Action
- Mandatory Field Change Order (FCO) 528 053 "Check for zinc plated Precise Table 'Z' mechanism fixation bolts", dated 1/11/2007 was distributed to all affected customers. The Change Order identified the product, stated the reason for the FCO, and the procedure to check and resolve the problem identified.
- Quantity
- 185 units
- Distribution
- Worldwide Distribution -- USA, Puerto Rico, Argentina, Australia, Austria, Bangladesh, Belgium, Canada, China, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iraq, Israel, Italy, Japan, Korea, Malaysia, Mexico, Netherlands, Pakistan, Peru, Poland, Russia, Serbia, Spain, Sudan, Sweden, Taiwan, Thailand, Turkey & United Kingdom.
- Lot, serial or model codes
- 103101, 105136, 105183, 105223, 105271, 105281, 105292, 105330, 105343, 105370, 105446, 105473, 105511, 105518, 105528, 105532, 105542, 105550, 105568, 151416, 151417, 151420, 151421, 151422, 151423, 151424, 151425, 151426, 151427, 151428, 151429, 151430, 151432, 151433, 151434, 151435, 151436, 151437, 151439, 151440, 151441, 151443, 151444, 151445, 151446, 151447, 151448, 151449, 151450, 151451, 151452, 151453, 151454, 151455, 151456, 151457, 151458, 151459, 151460, 151461, 151462, 151463, 151464, 151466, 151467, 151468, 151469, 151470, 151472, 151473, 151474, 151475, 151476, 151477, 151478, 151479, 151480, 151481, 151483, 151484, 151485, 151486, 151487, 151488, 151489, 151490, 151491, 151492, 151493, 151494, 151495, 151496, 151497, 151499, 151500, 151501, 151502, 151503, 151504, 151505, 151506, 151507, 151508, 151509, 151510, 151511, 151513, 151514, 151515, 151516, 151517, 151518, 151519, 151520, 151522, 151523, 151524, 151525, 151526, 151527, 151528, 151529, 151530, 151531, 151532, 151533, 151534, 151535, 151536, 151537, 151538, 151539, 151540, 151541, 151542, 151543, 151544, 151546, 151547, 151549, 151550, 151551, 151552, 151553, 151554, 151555, 151557, 151558, 151559, 151561, 151565, 151566, 151567, 151568, 151569, 151572, 151573, 151578, 151574, 151575, 151579, 151580, 151581, 151583, 151584, 151585, 151587, 151588, 151589, 151590, 151595, 151596, 151597, 151599, 151600, 151601, 151602, 151603, 151608, 151614, 151618, 151622, 151626, 151627, and 151628.
- 510(k) numbers
- ["K983678"]
- PMA numbers
- not on file
- Product code
- JAI
- Firm FEI
- 1037831
- Firm city
- Norcross
- Firm state
- GA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
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Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28