Class 2 Device Recall Ingenia 1.5T CX

• Date Initiated by Firm: October 23, 2023
• Date Posted: November 21, 2023
• Recall Status: Open, Classified
• Recall Number: Z-0392-2024
• Recall Event ID: 93361
• 510(K)Number: K052013 K052078 K063559 K162931 K173079
• Product Classification: System, nuclear magnetic resonance imaging - Product Code LNH
• Product: Ingenia 1.5T CX
• Code Information: Product No. 781261 & 781262; UDI-DI: (01)00884838068438(21)77008, (01)00884838068438(21)77016, (01)00884838068438(21)77018, (01)00884838068445(21)77032, (01)00884838068445(21)77034, (01)00884838068445(21)77035, (01)00884838068445(21)77038, (01)00884838068445(21)77040, (01)00884838068445(21)77041, (01)00884838068445(21)77046, (01)00884838068445(21)77049, (01)00884838068445(21)77050, (01)00884838068445(21)77054, (01)00884838068445(21)77056, (01)00884838068445(21)77058, (01)00884838068445(21)77059, (01)00884838068445(21)77061, (01)00884838068445(21)77062, (01)00884838068445(21)77065, (01)00884838068445(21)77066, (01)00884838068445(21)77067, (01)00884838068445(21)77071, (01)00884838068445(21)77072, (01)00884838068445(21)77074, (01)00884838068445(21)77075, (01)00884838068445(21)77078, (01)00884838068445(21)77081, (01)00884838068445(21)77083, (01)00884838068445(21)77084, (01)00884838068445(21)77087, (01)00884838068445(21)77093, (01)00884838068445(21)77094, (01)00884838068445(21)77097, (01)00884838068445(21)77100, (01)00884838068445(21)77101, (01)00884838068445(21)77106, (01)00884838068445(21)77109, (01)00884838068445(21)77110, (01)00884838068445(21)77111, (01)00884838068445(21)77119, (01)00884838068445(21)77120, (01)00884838068445(21)77121, (01)00884838068445(21)77124, (01)00884838068445(21)77126, (01)00884838068445(21)77129, (01)00884838068445(21)77130, (01)00884838068445(21)77131, (01)00884838068445(21)77137; Serial No. 77008, 77016, 77018, 77032, 77034, 77035, 77038, 77040, 77041, 77046, 77049, 77050, 77054, 77056, 77058, 77059, 77061, 77062, 77065, 77066, 77067, 77071, 77072, 77074, 77075, 77078, 77081, 77083, 77084, 77087, 77093, 77094, 77097, 77100, 77101, 77106, 77109, 77110, 77111, 77119, 77120, 77121, 77124, 77126, 77129, 77130, 77131, 77137.
• Recalling Firm/ Manufacturer: Philips North America Llc; 222 Jacobs St; Cambridge MA 02141-2289
• For Additional Information Contact: Customer Care Solutions Center; 1-800-722-9377
• Manufacturer Reason for Recall: Potential component failure in the Gradient Coil could product smoke and/or fire.
• FDA Determined Cause: Under Investigation by firm
• Action: The firm mailed URGENT Medical Device Correction Notices dated 10/23/2023 to consignees to notify them of this recall event. Consignees are instructed to identify if they possess any affected devices in their inventory and to follow the provided instructions for when scan aborts occur to prevent the failure mode associated with this recall event. Consignees are to stop the scan immediately and contact Philips Service if any of the failure situations outlined in the notice occur during a scan. Consignees are asked to complete and return the provided response form to Philips no later than 30 days after receipt of the recall notice. Questions can be directed to Customer Care Solutions at 1-800-722-9377.
• Quantity in Commerce: 48 units
• Distribution: 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.
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.

• 510(K) Database: 510(K)s with Product Code = LNH and Original Applicant = PHILIPS MEDICAL SYSTEMS; 510(K)s with Product Code = LNH and Original Applicant = PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.