Philips North America recalls Intera 1.5T Achieva Nova-Dual Product Number: 781173;
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the…
Read the official notice →- Date
- 2025-06-18
- Country
- United States
- Brand
- Philips
- Product
- Intera 1.5T Achieva Nova-Dual Product Number: 781173;
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Philips recalls
- 2025-10-01
USPhilips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice →- 2025-08-06
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Philips North America recalls Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (China ONLY);
The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
FDA · DevicePhilips North AmericaWorldwide distribution - US Nationwide and the countries of Albania, Algeria,…Official notice → - 2025-07-02
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Philips North America Llc recalls Spectral CT. Computed tomography X-ray system.
Devices with affected software may experience two unintended motion issues that may lead to contact between the Gantry or table with the operator or patient, along with additional software issues that affect CT…
FDA · DevicePhilips North America LlcDomestic: AZ, CA, CO, FL, GA, HI, IN, KY, MA, MD, MN, NY, OH, OR, PA, TX, VT,…Official notice → - 2025-05-28
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Philips North America Llc recalls Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Andorra,…Official notice → - 2025-05-14
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Philips North America Llc recalls Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm…
Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of AE, AL, AO, AR,…Official notice → - 2025-04-30
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Philips North America Llc recalls Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
Unintended motion issues related to Interventional Control that may lead to collision of the Gantry/table with the operator or patient.
FDA · DevicePhilips North America LlcWorldwide distribution: US (Nationwide); and OUS (Foreign) to countries of:…Official notice →
Other drugs & medical recalls in the United States
- 2025-06-18
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Stryker GmbH recalls Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.
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GE Medical Systems Information Technologies Inc recalls MUSE 5 Systems, Model Numbers 2021274-001, 2023032-005, 2027478-001, Large capacity client-server-based computer…
The MUSE Administrator Account active directory or local credential could potentially be used from your local network to log into a GE HealthCare MUSE 5 system and potentially manipulate recorded patient data.
FDA · DeviceGE Medical Systems Information Technologies IncWorldwide - US Nationwide distribution.Official notice → - US
Copan Italia recalls BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
Swabs for specimen collection may be prone to breakage during product usage.
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QUANTUM SURGICAL SAS recalls EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is a user controlled, stereotactic accessory intended to assist in the…
Due to a software bug the robotic arm may incorrectly guide the instrument compared to the planning defined by user.
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Beckman Coulter, Inc. recalls DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software versions 1.20
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Natus Neurology DBA Excel Tech., Ltd. (XLTEK) recalls Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box)…
Electrode placement labels on the Digital Acquisition Box (DAB) were applied backwards. This may ultimately lead to misdiagnosis of seizure location in neonates monitored with this device.
FDA · DeviceNatus Neurology DBA Excel Tech., Ltd. (XLTEK)Worldwide distribution - US Nationwide including Puerto Rico (PR) and OUS…Official notice →