🔍 RecallPedia

Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146

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) 781260, (2) 782112, (3) 782146; UDI-DI: (1) 00884838095076,(2) 00884838098886, (3) 00884838108691; Serial Numbers: (1) 10044, 10151, 10164, 10170, 11000, 11001, 11062, 11076, 12009, 18038, 18663, 18872, 18938, 20115, 20164, 20413, 21011, 21019, 21062, 21133, 21249, 21278, 21477, 21577, 21583, 21591, 21880, 21888, 22157, 22248, 32049, 32094, 32099, 32113, 32142, 32184, 32217, 32245, 32286, 32322, 32334, 32636, 32845, 39024, 5479, 5490, 8057, 8263, 8305, 8330, 8365, 8378, 8392, 8456, 8561, 8639, 8736, 8752, 8808, 8819, 8942, (2) 10479, 12002, 13024, 18651, 21205, 21685, 22267, 30031, 39106, (3) 13013, 20414, 21202, 21990, 22251, 32116, 32407, 32683, 33611, 39040;
  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: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146

Product Codes/Lot Numbers:

Model Numbers: (1) 781260, (2) 782112, (3) 782146; UDI-DI: (1) 00884838095076,(2) 00884838098886, (3) 00884838108691; Serial Numbers: (1) 10044, 10151, 10164, 10170, 11000, 11001, 11062, 11076, 12009, 18038, 18663, 18872, 18938, 20115, 20164, 20413, 21011, 21019, 21062, 21133, 21249, 21278, 21477, 21577, 21583, 21591, 21880, 21888, 22157, 22248, 32049, 32094, 32099, 32113, 32142, 32184, 32217, 32245, 32286, 32322, 32334, 32636, 32845, 39024, 5479, 5490, 8057, 8263, 8305, 8330, 8365, 8378, 8392, 8456, 8561, 8639, 8736, 8752, 8808, 8819, 8942, (2) 10479, 12002, 13024, 18651, 21205, 21685, 22267, 30031, 39106, (3) 13013, 20414, 21202, 21990, 22251, 32116, 32407, 32683, 33611, 39040;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1788-2025

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