Axiom Artis MP X-Ray System
This recall has been terminated (originally issued May 11, 2005).
- Recall Initiated
- April 1, 2005
- Posted
- May 11, 2005
- Terminated
- August 18, 2005
- Recall Number
- Z-0818-05
- Quantity
- 21 units
- Firm Location
- Malvern, PA
- Official Source
- View on FDA website ↗
Reason for Recall
potential problem with the fluoroscopy switch on the power grip
Distribution
The products were shipped to hospitals in AL, AZ, DC, DE, IA, MI, NC, NE, PA, RI, TX, WA, and WI.
Lot / Code Info
Serial numbers 10, 1021, 1025, 1026, 1027, 1043, 1044, 1048, 1050, 1052, 1056, 1065, 1067, 1069, 1080, 1082, 1083, 1085, 1087, 1089, and 1097.
Root Cause
Other
Action Taken
The recalling firm''s Customer Service Engineers are visiting each account to correct/replace the Power Grip button.
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