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Philips North America Llc recalls Intera 1.5T Power/Pulsar

Recalled November 29, 2023 · FDA recall Z-0394-2024 · Philips North America

Hazard
Potential component failure in the Gradient Coil could product smoke and/or fire. · FDA Class II
Units
1 unit
Sold at
Domestic: Nationwide Distribution; Foreign: Albania, Andorra, Argentina, Australia, Austria, Bangladesh, Belarus, Belgium, Bolivia, Bosnia, Brazil, Canada, Chile, China, Colombia, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Lebanon, Libya, Luxembourg, Malaysia, Malta, Mexico, Myanmar, Nepal, Netherlands, New Zealand, Norway, Pakistan, Panama, Peru, Poland, Portugal, Puerto Rico, Romania, Russian Fed., Rwanda, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, South Korea, Spain, Sudan, Sweden, Switzerland, Taiwan, Thailand, Turkey, Ukraine, United Kingdom, United States, UAE, Venezuela, Vietnam, & Yemen.

Description

Potential component failure in the Gradient Coil could product smoke and/or fire.

Product
Intera 1.5T Power/Pulsar
Manufacturer(s)
Philips North America Llc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Philips North America Llc recalls Intera 1.5T Power/Pulsar | RecallWatchUSA