GE Healthcare Revolution CT., multi-slice (256 detector row) CT scanner.
FDA Recall #Z-0985-2015 — Class II — December 19, 2014
Product Description
GE Healthcare Revolution CT., multi-slice (256 detector row) CT scanner.
Reason for Recall
Potential safety issue due to a required torque check on three bolted joints of the Revolution CT scanner. No injuries or illnesses reported.
Recalling Firm
GE Healthcare — Waukesha, WI
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
13 (7 US, 6 OUS)
Distribution
US: FL, WA, IL, UT, NY, CA. OUS: Canada, France, Hong Kong, Japan, Switzerland, United Arab Emirates.
Code Information
Mfg Lot or Serial # System ID 00000437461CN7 519646REVO1 00000437837CN8 M2322254 00000438342CN8 828210096 00000437028CN4 REV001 00000438864CN1 900010CT06 00000439199CN1 260010CT19 00000439068CN8 AE1477CT01 00000437787CN5 786596WKRIVO 00000438503CN5 206598REV1 00000438951CN6 309655REVCT 00000439029CN0 801662REV1 00000439160CN3 212241REVCT 00000439367CN4 415476MCT3
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated