Philips North America Llc recalls Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.
Potential for a plan box not updated issue during Interventional procedure with Spectral CT that may lead to a collision with the operator or with the needle placed inside the patient, and an incorrect patient ID…
Read the official notice →- Date
- 2024-12-11
- Country
- United States
- Brand
- Philips
- Product
- Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of AR, AZ, CA, FL, GA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2025-04-23
USPhilips North America Llc recalls Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
Potential for collimator to fall as a result of incorrect installation.
FDA · DevicePhilips North America LlcWorldwide - US Nationwide distribution in the states of AK, FL, KS, MS, NH,…Official notice →- 2025-02-12
- US
Philips North America Llc recalls IntelliVue Patient Monitor MX400. Model Number: 866060
Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.
FDA · DevicePhilips North America LlcUS distribution to Florida, North Carolina, and Oregan. International…Official notice → - 2024-12-25
- US
Philips North America Llc recalls Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216
The following four issues are included: 1. Certain Channel Settings may result in an Access Point preventing a connected client device from roaming to another Access Point potentially causing the client device to…
- 2024-12-04
- US
Philips North America Llc recalls dS Breast 16ch 1.5T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-10-16
- US
Philips North America recalls Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1
During extended operation of the MX40 with the PIC iX, the DHCP (Dynamic Host Configuration Protocol) lease can expire on the MX40. If the DHCP lease expires while the device is offline, upon reconnecting with the PIC…
- US
Philips North America Llc recalls IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2 are affected as follows:…
Devices with Option CP2 and initially programmed to software version P.01.01 were configured incorrectly at the factory. Therefore, Enhanced ECG Capabilities provided by Option CP2 were not enabled in these devices.…
FDA · DevicePhilips North America LlcForeign Only: Denmark France Germany Japan United KingdomOfficial notice →
Other drugs & medical recalls in the United States
- 2024-12-11
- US
Cartiva, Inc recalls Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)
Patients implanted with synthetic cartilage implant, may experience a higher-than expected occurrence rate of the following hazards: revision, removal, implant subsidence, displacement, pain, nerve damage or…
FDA · DeviceCartiva, IncWorldwide - US Nationwide distribution in the states of CO, CT, FL, IL, MI,…Official notice → - US
Siemens Healthcare Diagnostics, Inc. recalls Atellica CI Analyzer. Catalog Numbers: 10947347.
Potential that the IMT Diluent volume remaining (% remaining) does not decrease as expected on the Atellica CI Analyzer, potentially leading to the IMT Diluent being empty while still displaying that volume is…
FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide and the countries of Austria,…Official notice → - US
Becton Dickinson & Co. recalls BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990
BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is…
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of Algeria,…Official notice → - US
Wilson-Cook Medical Inc. recalls Cook Medical HEMO-7-EU Hemospray Endoscopic Hemostat, REF G24663, 2.8 cm, sterile.
Specific lots of product have been manufactured with nonconforming raw materials resulting in the red activation knob cracking or breaking at the activation knob internal threading while the device is activated.
FDA · DeviceWilson-Cook Medical Inc.Distribution was OUS only to Argentina, Brazil, and Israel.Official notice → - US
Smith & Nephew Inc. recalls BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.
Sterile barrier breach due to inadequate packaging design that could not hold the geometry of the device.
FDA · DeviceSmith & Nephew Inc.Worldwide - US Nationwide distribution in the states of AK, AL, IL, IN, KY,…Official notice → - US
Orthoscan, Inc. recalls Ziehm Solo. Digital Mobile C-arm
Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand…