PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Zenition 50, Model Number: 718096

Recalled November 20, 2024 · FDA recall Z-0352-2025 · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V

Hazard

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure. · FDA Class II

Units

986 units (156 US, 29 Canada, 801 ROW)

Sold at

Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Bolivia, Brazil, Bulgaria, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, El Salvador, Estonia, Faroe Islands, Fiji, Finland, France, French Guiana, Germany, Gibraltar, Greece, Guatemala, Hong Kong, Hungary, Iceland, India, Indonesia, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of, Kuwait, Lao People's Democratic Republic, Lebanon, Lithuania, Malaysia, Malta, Martinique, Mauritius, Mexico, Morocco, Myanmar, Netherlands, New Zealand, Nicaragua, Nigeria, Norway, Pakistan, Palestine, State of, Panama, Peru, Philippines, Poland, Portugal, R¿union, Romania, Russian Federation, Rwanda, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Suriname, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uzbekistan, Viet Nam, Yemen.

Description

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

Product

Philips Zenition 50, Model Number: 718096

Manufacturer(s)

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Made in

Netherlands

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