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Recall Observatory FDA recall evidence

Device product

GE Healthcare Innova IGS 540. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.

Z-1982-2015

May 29, 2015

Class II

Product summary

Firm
GE Healthcare
Event
Event 71508
Status
Terminated
Classification
Class II
Quantity
6
Official record key
device-enforcement:Z-1982-2015

Official wording

Reason: GE Healthcare has recently become aware of a potential safety issue that may result in the loss of C-arm gantry motion capability on fluoroscopic Interventional imaging systems (Innova, Optima and Discovery).

Code information: Serial Number System ID 0000012C2S0118 850862IGS 0000013C2S0207 352333VASC2 15C2R0063 GON4244211 15C2R0068 210297GE540 15C2R0053 804323IGS540 0000015C2R0059 0828160013

Distribution pattern: Worldwide Distribution: US (nationwide) including states of: CA, DE, FL, GA, IL, IN, KS, MS, NV, OH, OK, OR, PA, TN, TX, VA, WA and WI; and countries of: ARGENTINA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, FRANCE, GERMANY, HONG KONG, HUNGARY, INDIA, INDONESIA, ITALY, JAPAN, RUSSIA, UNITED KINGDOM, and VIETNAM.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    GE Healthcare has recently become aware of a potential safety issue that may result in the loss of C-arm gantry motion capability on fluoroscopic Interventional imaging systems (Innova, Optima and Discovery).