December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD BACTEC FX, Instrument Top, Packaged Version or Model: 441385 Catalog Number: 441385
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD Phoenix M50 Automated Microbiology System Version or Model: 443624 Catalog Number: 443624
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD Synapsys Informatics Solution (Laboratory Solution) Version or Model: 444150 Catalog Number: 444150
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD MAX System, BD MAX Instrument Version or Model: 441916 Catalog Number: 441916
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD EpiCenter Data Management System, Multi User Software Version or Model: 440981 Catalog Number: 440981
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD EpiCenter Data Management System Version or Model: 440887 Catalog Number: 440887
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Becton Dickinson & Co. recalls BD EpiCenter Single User Software Version or Model: 441007 Catalog Number: 441007
Hazard: 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 a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
December 11, 2024Medical DevicesFDA
Philips North America Llc recalls Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.
Hazard: 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 software issue that may lead to misdiagnosis.
December 11, 2024Medical DevicesFDA
Wilson-Cook Medical Inc. recalls Cook Medical HEMO-7-EU Hemospray Endoscopic Hemostat, REF G24663, 2.8 cm, sterile.
Hazard: 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.
December 11, 2024Medical DevicesFDA
Smith & Nephew Inc. recalls BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.
Hazard: Sterile barrier breach due to inadequate packaging design that could not hold the geometry of the device.
December 11, 2024Medical DevicesFDA
Orthoscan, Inc. recalls Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system
Hazard: 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 switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
December 11, 2024Medical DevicesFDA
Orthoscan, Inc. recalls Ziehm Vision RFD. Interventional fluoroscopic x-ray system
Hazard: 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 switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
December 11, 2024Medical DevicesFDA
Orthoscan, Inc. recalls Ziehm Vision R. Iterventional fluoroscopic x-ray system
Hazard: 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 switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
December 11, 2024Medical DevicesFDA
Orthoscan, Inc. recalls Ziehm Vision FD. Interventional fluoroscopic x-ray system
Hazard: 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 switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
December 11, 2024Medical DevicesFDA
Orthoscan, Inc. recalls Ziehm Vision system, x-ray, tomography, computed.
Hazard: 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 switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
December 11, 2024Medical DevicesFDA
Orthoscan, Inc. recalls Ziehm Solo FD. Interventional fluoroscopic x-ray system
Hazard: 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 switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
December 11, 2024Medical DevicesFDA
Orthoscan, Inc. recalls Ziehm Solo. Digital Mobile C-arm
Hazard: 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 switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
December 11, 2024Medical DevicesFDA
WINGDERM ELECTRO-OPTICS LTD. recalls Diode Laser Hair Removal model: WLA-01
Hazard: All model WLA-01 systems sold to US customers are found to have labeling non-compliances
December 11, 2024Medical DevicesFDA
WINGDERM ELECTRO-OPTICS LTD. recalls Non-ablative Fractional Laser Systems, Model: WFB-01
Hazard: Model WFB-01 sold to US customers before Aug 23, 2022 has been found to have a software bug (6 units). All WFB-01 models sold to US customers found to have labeling non-compliances (22 units)
December 11, 2024Medical DevicesFDA
Epilog Laser Corp. recalls Fusion Pro 24, Model 17000
Hazard: a. A small number of Fusion Pro 24 units were released with an incorrectly placed Interlock device. As a result, the system can be operated with the front-loading door in an open position. b. Fails to comply with Class 2 designation, indicated in Part 6 of Laser Product Report. An incorrectly placed Interlock device can allow Class 4 laser radiation fields during operation.
December 4, 2024Medical DevicesFDA
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV35
Hazard: Mobile x-ray system receiving/storage(operation) requirements to be followed: Temp:14 to 131(50 to 86) degrees F, RH:10% to 86%(30% to 60%) allow condensation dry time, Atmospheric Pressure:50kPa to 106 kPa(70kPa to 106kPa), Altitude:-102ft to 12,000 ft, (Maximum Gradient:9 degrees Fahrenheit), which mitigate risk of capacitor malfunction, unpredictable behavior, overheating, unintended start-up.
December 4, 2024Medical DevicesFDA
Gauthier Biomedical, Inc. recalls TriALTIS TORQUE LIMITER, RATCHET, 11.3 Nm, Model Number 5161-00-5048 (G919509)
Hazard: An out of specification component may result in the device exhibiting torque output higher than the design specification.
December 4, 2024Medical DevicesFDA
LivaNova Deutschland GmbH recalls Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software
Hazard: Heart-Lung Machine GUI touchscreen may go dark for 10-15 seconds, safety/performance functions remain operational before reset, control maintained through backup control panel, but second reset may occur, may lead to gas blender standby, then gas blender must be reactivated using user interface on blender, sensors deactivated until new case started; GUI reset can lead to Hypoxia and Hypoperfusion.
December 4, 2024Medical DevicesFDA
Securitas Healthcare LLC recalls Arial Server Software Versions 11.1.4 through 11.1.6, SKU 54305, in conjunction with the Arial Mobile Application or Ari
Hazard: Certain software versions will not notify end users of calls initiated by call points with the Arial Emergency and Nurse Call System.
December 4, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialy
Hazard: There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.