Z-2055-2021 Class II Ongoing
FDA device recall Z-2055-2021 was initiated by GE Healthcare, LLC on June 4, 2021 and is designated Class II. Reason for recall: GE Healthcare has recently become aware of an issue on the affected products listed below where the "Patient Orientation" button may inadvertently be clicked when intending to click on the "Save RX" b… The recall status is ongoing. Affected quantity: 585 devices.
Recall Details
- Product Type
- Devices
- Report Date
- July 21, 2021
- Initiation Date
- June 4, 2021
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 585 devices
Product Description
Discovery MR750w 3.0T - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
Reason for Recall
GE Healthcare has recently become aware of an issue on the affected products listed below where the "Patient Orientation" button may inadvertently be clicked when intending to click on the "Save RX" button. This changes the prescribed patient orientation on the system prior to running the initial 3-Plane Localizer Scan (See Figure 1 for reference to buttons.) Selecting and saving a patient orientation that does not match the patient's actual position may result in incorrectly annotated and/or flipped images.
Distribution Pattern
Worldwide distributions.