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Open, Classified

Philips Zenition 50, Model Number: 718096

FDA Recall Z-0352-2025 · Posted 2024-11-12

Recall StatusOpen, Classified
Product CodeOWB
Date Initiated2024-10-07
Product Quantity986 units (156 US, 29 Canada, 801 ROW)

Reason for Recall

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

Firm Action

On October 7, 2024 URGENT MEDICAL DEVICE CORRECTION letters were sent to consignees. 4. Actions that should be taken by the customer! user in order to prevent risks for patients. " Affected systems may continue to be used in accordance with their intended use and Instructions for Use (IFU). " Establish emergency protocols including back up devices if available in place to manage the situation should you experience this issue during the procedure. " Circulate this Urgent Medical Device Correction to all users of the system so that they are aware of the issue. " Keep this Urgent Medical Device Correction with the documentation of the system until Philips implements the correction in your system. Ensure that the letter is in a place likely to be seen! viewed. " If you experience a power loss issue with your system, report the event to Philips. " Complete and return the attached response form (on page 04) to Philips promptly and no later than 30 days from receipt. Completing this form confirms receipt of the Urgent Medical Device Correction and understanding of the issue and required actions to be taken. 5. Actions planned by Philips IGT (Image Guided Therapy) systems to correct the problem Philips will replace the 5-Ampere MCU board fuse with a 10-Ampere MCU board fuse in all affected systems. Philips will contact customers to schedule a visit to perform this action free of charge (reference FC071800109). This notice has been reported to the appropriate Regulatory Agencies. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA s MedWatch Adverse Event Reporting program either online, or by regular mail, or by fax. Be assured that maintaining a high level of safety and quality is our highest priority. If you need additional information or support concerning this issue, contact your local Philips representative at 1800-722-9377 (Philips Customer Care Solutions Center).

Root Cause

Under Investigation by firm

Distribution Pattern

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.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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