Philips North America Llc GYROSCAN T5, Magnetic Resonance System. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GYROSCAN T5, Magnetic Resonance System.
Brand
Philips North America Llc
Lot Codes / Batch Numbers
Model No. 78104, UDI-DI n/a, Serial No. 605, 889, 915, 938, 663, 600, 891.
Products Sold
Model No. 78104; UDI-DI n/a; Serial No. 605, 889, 915, 938, 663, 600, 891.
Philips North America Llc is recalling GYROSCAN T5, Magnetic Resonance System. due to Patient support table floor plate may be incorrectly installed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Patient support table floor plate may be incorrectly installed.
Recommended Action
Per FDA guidance
Consignees were mailed an URGENT Medical Device Correction notice, dated 3/12/24. Consignees are instructed by the notice to identify affected systems, which can continue to be used with the provided instruction. If a patient's weight is at or near the maximum load of the device take care that they do not sit on the end of the tabletop opposite the bore entrance and that they do not hop down from their sitting position while the support is at its highest position. If the affected system has any unexpected movement or becomes unstable immediately stop use and contact your Philips representative for interim support. The recall notice is to be circulated to all users and the provided advisory displayed. Completed response forms are to be emailed to pd.cnr@philips.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026