Recall Z-0198-2013— GE Healthcare, LLC
Class II · Terminated
Class II FDA medical device recall by GE Healthcare, LLC, initiated 2012-09-20, terminated 2013-12-05. FDA's recall record names no specific 510(k) clearance for this event. Product: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging of the human head and body.. Reason: It was discovered GE Healthcare has become aware of a firmware issue on the mobile radiographic product, Brivo XR285amx, Optima XR200amx, Optima XR22Oamx and Optima XR200amx with Digital Upgrade, related to Technique Accuracy as mandated by the US Code of Federal Regulations (21CFR) and IEC 60601-2-54..
- Recalling firm
- GE Healthcare, LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2012-09-20
- Terminated
- 2013-12-05
- Firm location
- Waukesha, WI, United States
Product description
GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging of the human head and body.
Reason for recall
It was discovered GE Healthcare has become aware of a firmware issue on the mobile radiographic product, Brivo XR285amx, Optima XR200amx, Optima XR22Oamx and Optima XR200amx with Digital Upgrade, related to Technique Accuracy as mandated by the US Code of Federal Regulations (21CFR) and IEC 60601-2-54.
Data sourced from openFDA. This site is unofficial and independent of the FDA.