🔍 RecallPedia

Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;

Class I - Dangerous
🏥 Medical Devices Recalled: May 13, 2025 Philips North America Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Numbers: (1) 782110, (2) 782152; UDI-DI: (1) 00884838099364, (2) 00884838112841; Serial Numbers: (1) 63007, 63011, 63022, 63043, 63047, 63050, 63051, 63060, 63074, 63078, 63079, 63082, 63085, 63090, 63095, 63097, 63100, 63116, 63121, 63132, 63136, 63137, 63142, 63143, 63144, 63146, 63150, 63156, 63160, 63162, 63166, 63190, 63202, 63210, 63222, 63226, 63228, 63235, 63238, 63239, 63244, 63247, 63258, 63262, 63263, 63264, 63265, 63266, 63267, 63268, 63269, 63270, 63272, 63274, 63275, 63276, 63281, 63282, 63283, 63284, 63285, 63286, 63287, 63288, 63289, 63290, 63292, 63300, 63303, 63304, 63305, 63306, 63307, 63337, 63352, 63356, 63361, 63363, 63366, 63367, 63370, 63372, 63394, 63456, 63596, 63599, (2) 69000, 69003, 69004, 69005, 69006, 69007, 69008, 69010, 69011, 69012, 69014, 69015, 69016, 69017, 69019, 69020, 69021, 69022, 69023, 69024, 69026, 69027, 69029, 69031, 69032, 69034, 69036, 69037, 69041, 69043, 69044, 69045, 69046, 69048, 69051, 69052, 69053, 69055, 69056, 69058, 69060, 69061, 69063, 69064, 69065, 69066, 69067, 69068, 69069, 69070, 69071, 69072, 69073, 69075, 69076, 69077, 69078, 69080, 69081, 69082, 69085, 69086, 69087, 69089, 69092, 69093, 69094, 69095, 69096, 69097, 69098, 69100, 69102, 69103, 69106, 69107, 69110, 69111, 69112, 69115, 69116, 69121, 69122, 69123, 69124, 69126, 69127, 69130, 69131, 69133, 69136, 69137, 69141, 69147, 69150, 69161, 69170, 69171, 69172, 69176;
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Philips North America Llc
Reason for Recall:
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;

Product Codes/Lot Numbers:

Model Numbers: (1) 782110, (2) 782152; UDI-DI: (1) 00884838099364, (2) 00884838112841; Serial Numbers: (1) 63007, 63011, 63022, 63043, 63047, 63050, 63051, 63060, 63074, 63078, 63079, 63082, 63085, 63090, 63095, 63097, 63100, 63116, 63121, 63132, 63136, 63137, 63142, 63143, 63144, 63146, 63150, 63156, 63160, 63162, 63166, 63190, 63202, 63210, 63222, 63226, 63228, 63235, 63238, 63239, 63244, 63247, 63258, 63262, 63263, 63264, 63265, 63266, 63267, 63268, 63269, 63270, 63272, 63274, 63275, 63276, 63281, 63282, 63283, 63284, 63285, 63286, 63287, 63288, 63289, 63290, 63292, 63300, 63303, 63304, 63305, 63306, 63307, 63337, 63352, 63356, 63361, 63363, 63366, 63367, 63370, 63372, 63394, 63456, 63596, 63599, (2) 69000, 69003, 69004, 69005, 69006, 69007, 69008, 69010, 69011, 69012, 69014, 69015, 69016, 69017, 69019, 69020, 69021, 69022, 69023, 69024, 69026, 69027, 69029, 69031, 69032, 69034, 69036, 69037, 69041, 69043, 69044, 69045, 69046, 69048, 69051, 69052, 69053, 69055, 69056, 69058, 69060, 69061, 69063, 69064, 69065, 69066, 69067, 69068, 69069, 69070, 69071, 69072, 69073, 69075, 69076, 69077, 69078, 69080, 69081, 69082, 69085, 69086, 69087, 69089, 69092, 69093, 69094, 69095, 69096, 69097, 69098, 69100, 69102, 69103, 69106, 69107, 69110, 69111, 69112, 69115, 69116, 69121, 69122, 69123, 69124, 69126, 69127, 69130, 69131, 69133, 69136, 69137, 69141, 69147, 69150, 69161, 69170, 69171, 69172, 69176;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1804-2025

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