Recall Z-1557-2024— 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: Enterprise 1.5T, 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
Enterprise 1.5T, 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.