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Other Medical Devices

🏥 Medical Devices 15,203 recalls

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Aug 8, 2025 Other Medical Devices Nationwide View Details →

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Aug 8, 2025 Other Medical Devices Nationwide View Details →

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Aug 8, 2025 Other Medical Devices Nationwide View Details →

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Aug 8, 2025 Other Medical Devices Nationwide View Details →

Medtronic MiniMed, Inc. is recalling InPen App for iOS and Android users due to software design errors that could lead to a missed short-acting insulin dose reminder and a recommendation to correct a high glucose value. It does not impact insulin delivery, long-acting insulin dose reminders, or CGM alerts, and users can still use the pen itself to calculate a dose, deliver insulin, record the dose date/time, and view CGM data. This issue was identified during internal testing before release in the US but after release to OUS customers, no complaints or MDRs related to this recall have been reported. Use of the affected device may result hyperglycemia by failing to alert the user and delay treatment of diabetes.

Jun 16, 2025 Other Medical Devices View Details →

Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.

Aug 6, 2025 Other Medical Devices View Details →

Due to an incorrect test results provided that indicated the incorrect drug therapy recommendation

Jun 17, 2025 Other Medical Devices Nationwide View Details →

Packaging failures were identified which could lead to a breach in the sterile barrier.

Aug 5, 2025 Other Medical Devices Nationwide View Details →

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Aug 8, 2025 Other Medical Devices Nationwide View Details →

Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.

Aug 1, 2025 Other Medical Devices Nationwide View Details →

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Jul 10, 2025 Other Medical Devices Nationwide View Details →

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Aug 8, 2025 Other Medical Devices Nationwide View Details →

FloPatch FP120, REF: FP120-FOT01-005

Flosonics Medical (R/A 1929803 ONTARIO CORP.)

Class I - Dangerous

Flowmeter patch as a human readable expiry date on the outer shipping packaging that reads 2025-06-20 when it should read 2026-06-20.

Aug 7, 2025 Other Medical Devices Nationwide View Details →

Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.

Aug 1, 2025 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Jul 10, 2025 Other Medical Devices Nationwide View Details →