Recall StatusTerminated
Date Initiated2016-05-09
Date Terminated2018-09-04
Product Quantity197 (US = 68; OUS = 129)
Reason for Recall
GEHC has become aware of a potential safety issue in the Revolution CT Patient Table that can result in unintended motion in cases involving large patients. The Revolution CT cradle can descend on its own after activation by the user. This can put the patient at risk for harm. The harm can involve the impinging or crushing of a hand if caught between the cradle and CT inner gantry bore. No injurie
Firm Action
The firm, GE Healthcare, sent an "Urgent Medical Device Correction" letter ,GEHC Ref# 25468, dated May 9, 2016 to its Consignees. The letter was addressed to Hospital Administrators / Risk Managers, Radiology Department Managers & Radiologists. The letter described the Safety Issue, Safety Instructions, Affected Product Details, Product Correction & Contact Information. The consignees were instructed to ensure that all potential users in your facility are made aware of this safety notification and the recommended actions; continue to use your Revolution CT product; follow the Patient Positioning warning outlined in the Revolution CT User Manual; to prevent pinching or crushing of the patients extremities, keep the patients hands and feet away from the edge of the moving table top/cradle and its surrounding equipment, or between table base and side panels of the table; and take special care when positioning physically large patients.
If you have any questions or concerns regarding this notification, please contact GE Healthcare Service at 1-800-437-1171 or your local Service Representative.
Root Cause
Process control
Distribution Pattern
Worldwide Distribution: US (nationwide) including states of: AL, CA, CT, FL, GA, HI, IL, IN, KS, NE, NY,NC, OH, OR, PA, TN, TX, UT, A, WA, WI; and countries of: Australia, Belgium, Brazil, Canada, China, Denmark, Estonia, France, Germany, Hong Kong, Indonesia, Italy, Japan, Korea (Republic of), Kuwait, Mexico, New Zealand, Norway, Peru, Poland, Saudi Arabia, Singapore, Spain, Sweden, Switzerland, Taiwan, United Arab Emirates, and United Kingdom.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.