Revolution Apex, Revolution CT with Apex Edition
Reported: April 13, 2022 Initiated: June 30, 2021 #Z-0815-2022
Product Description
Revolution Apex, Revolution CT with Apex Edition
Reason for Recall
The accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
Details
- Recalling Firm
- GE Healthcare, LLC
- Units Affected
- 273 (51 US, 222 OUS) in total
- Distribution
- Worldwide - US Nationwide distribution.
- Location
- Waukesha, WI
Frequently Asked Questions
What product was recalled? ▼
Revolution Apex, Revolution CT with Apex Edition. Recalled by GE Healthcare, LLC. Units affected: 273 (51 US, 222 OUS) in total.
Why was this product recalled? ▼
The accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 13, 2022. Severity: Moderate. Recall number: Z-0815-2022.
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