AIRO Mobile CT System recall
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed tomography applications for anatomy…
Why was AIRO Mobile CT System recalled?
Risk of unintended motion while the AIRO system is in transport mode.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All units released since April 2014. Serial numbers: AIRO-2251 AIRO-2328 AIRO-2344 AIRO-2324 AIRO-2346 AIRO-0106 AIRO-0107-R AIRO-0108 AIRO-0109 AIRO-0110 AIRO-0111 AIRO-0112 AIRO-0113 AIRO-0114 AIRO-0115 AIRO-0116 AIRO-0117 AIRO-0118 AIRO-0119 AIRO-0120 AIRO-0121 AIRO-0122 AIRO-0124 AIRO-0125 AIRO-0126 AIRO-0127 AIRO-0128 AIRO-0129 AIRO-0130 AIRO-0131 AIRO-0132 AIRO-0133 AIRO-0134 AIRO-0136 AIRO-0137 AIRO-0138 AIRO-0139 AIRO-0140 AIRO-0141 AIRO-0142 AIRO-0143 AIRO-0144 AIRO-0145 AIRO-0146 AIRO-0148 AIRO-0149 AIRO-0151 AIRO-0152 AIRO-0153 AIRO-0154 AIRO-0155 AIRO-0156 AIRO-0157 AIRO-0158 AIRO-0159 AIRO-0160 AIRO-0161 AIRO-0162 AIRO-0163 AIRO-0164 AIRO-0165 AIRO-0166 AIRO-0167 AIRO-0168 AIRO-0170 AIRO-0172 AIRO-0174 AIRO-0175 AIRO-0176 AIRO-0177 AIRO-0178 AIRO-0180 AIRO-0181 AIRO-0182 AIRO-0184 AIRO-0186 AIRO-0187 AIRO-0188 AIRO-0189 AIRO-0190 AIRO-0191 AIRO-0192 AIRO-0193 AIRO-0194 AIRO-0195 AIRO-0196 AIRO-0197 AIRO-0198 AIRO-0199 AIRO-0200 AIRO-0201 AIRO-0202 AIRO-0203 AIRO-0204 AIRO-0205 AIRO-0206 AIRO-0207 AIRO-0211 AIRO-0212 AIRO-0213 AIRO-0214 AIRO-0216
- Product
- AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed tomography applications for anatomy…
- Recalling firm
- Brainlab AG
- Quantity
- 102
- Distribution
- Worldwide Distribution - US Nationwide in the U.S. States: of AK, AZ, CA, CO, FL, GA, IL, KY, LA, MD, MA, MI, MN, MT, MO, NJ, NY, NC, OH, PA, RI, TN, TX, UT, VA, WA, and WV; and the countries of Argentina, Australia, Austria, Belgium, Canada, Egypt, France, Germany, India, Italy, Japan, Kazakhstan, Lithuania, Netherlands, Saudi Arabia, Spain, Switzerland, United Arab Emirates, and Uzbekistan.
- Recall date
- February 14, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)