Philips Medical Systems (Cleveland) Inc Intinion 1.5 T MRI Scanner. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Intinion 1.5 T MRI Scanner.
Brand
Philips Medical Systems (Cleveland) Inc
Lot Codes / Batch Numbers
Serial Numbers ZA101-ZA188, ZA190-192, ZA195, ZA200, ZA201.
Products Sold
Serial Numbers ZA101-ZA188, ZA190-192, ZA195, ZA200, ZA201.
Philips Medical Systems (Cleveland) Inc is recalling Intinion 1.5 T MRI Scanner. due to There is a potential for the patient to be exposed to cryogenic fluids (liquid air) dripping from the vent during a quench due to the location of the . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a potential for the patient to be exposed to cryogenic fluids (liquid air) dripping from the vent during a quench due to the location of the vent.
Recommended Action
Per FDA guidance
A Mandatory Service Letter, dated April 17, 2003, was sent to service technicians instructing the technicans to perform a mandatory safety modification.
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