GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system
Reported: June 21, 2017 Initiated: May 19, 2017 #Z-2194-2017
Product Description
GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system
Reason for Recall
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
Details
- Recalling Firm
- GE Healthcare, LLC
- Units Affected
- 10,884
- Distribution
- Worldwide Distribution - USA (nationwide) including Puerto Rico and to the countries of : Japan, Jordan, Kazakhstan, Korea ( Republic of) Kuwait, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritania, Mexico, Moldova, Morocco, Nambia, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Republic of Serbia, Reunion, Romania, Russia, Rwanda, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, Spain Sweden, Switzerland, Syria, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Venezuela, Vietam and Yemen.
- Location
- Waukesha, WI
Frequently Asked Questions
What product was recalled? ▼
GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system. Recalled by GE Healthcare, LLC. Units affected: 10,884.
Why was this product recalled? ▼
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 21, 2017. Severity: Moderate. Recall number: Z-2194-2017.
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