Recall Z-1559-2024— Philips North America Llc
Class II · Ongoing
Class II FDA medical device recall by Philips North America Llc, initiated 2024-03-12. FDA's recall record names no specific 510(k) clearance for this event. Product: GYROSCAN ACS-NT, Magnetic Resonance System.. Reason: Patient support table floor plate may be incorrectly installed..
- Recalling firm
- Philips North America Llc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-03-12
- Firm location
- Cambridge, MA, United States
Product description
GYROSCAN ACS-NT, Magnetic Resonance System.
Reason for recall
Patient support table floor plate may be incorrectly installed.
Data sourced from openFDA. This site is unofficial and independent of the FDA.