By

Amy Sellers
Company:Roche Diabetes Care, Inc. Date of Enforcement Report 2/21/2018 Class lI: PRODUCT Accu-Chek Connect Diabetes Management App, Catalog number 07562462001 / GTIN number 00365702700000 & Catalog number 07250452001 / GTIN number 00365702700017 Recall Number Z-0625-2018 REASON Certain iOS and Android App versions contain a program error (bug) in the Bolus Advisor feature. Due to a...
Read More
Company:Philips Medical Systems (Cleveland) Inc Date of Enforcement Report 2/21/2018 Class lI: PRODUCT Ingenuity TF PET/CT (model 882442) running software version 4.0.2This device is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem produces cross-sectional images of the body by computer reconstruction of x-ray transmission...
Read More
Company:Philips Medical Systems (Cleveland) Inc Date of Enforcement Report 2/14/2018 Class lI: PRODUCT Philips Brilliance 64 computed tomography x-ray system Recall Number Z-0518-2018 REASON Numerous issues related to software Brilliance iCT 4.1.6 software version. RECALLING FIRM/MANUFACTURER Philips Medical Systems (Cleveland) Inc, Cleveland, OH on 10/6/2017. Voluntary: Firm Initiated recall is ongoing. VOLUME OF PRODUCT IN...
Read More
Company:Philips Medical Systems (Cleveland) Inc Date of Enforcement Report 2/14/2018 Class lI: PRODUCT Philips Ingenuity Core 128 computed tomography x-ray system Recall Number Z-0520-2018 REASON Numerous issues related to software Brilliance iCT 4.1.6 software version. RECALLING FIRM/MANUFACTURER Philips Medical Systems (Cleveland) Inc, Cleveland, OH on 10/6/2017. Voluntary: Firm Initiated recall is ongoing. VOLUME OF PRODUCT...
Read More
Company:Spacelabs Healthcare Date of Enforcement Report 2/14/2018 Class lI: PRODUCT Spacelabs Healthcare Xhibit Telemetry Receiver, Model 96280, software version 1.1, Recall Number Z-0532-2018 REASON Spacelabs has received multiple complaints reporting telemetry beds dropping off the Spacelabs Central Station resulting in a loss of monitoring. RECALLING FIRM/MANUFACTURER Spacelabs Healthcare Inc., Snoqualmie, WA on 1/17/2018. Voluntary: Firm...
Read More
Company:Philips Medical Systems (Cleveland) Inc Date of Enforcement Report 2/14/2018 Class lI: PRODUCT Philips Ingenuity Core computed tomography x-ray system Recall Number Z-0519-2018 REASON Numerous issues related to software Brilliance iCT 4.1.6 software version. RECALLING FIRM/MANUFACTURER Philips Medical Systems (Cleveland) Inc, Cleveland, OH on 10/6/2017. Voluntary: Firm Initiated recall is ongoing. VOLUME OF PRODUCT IN...
Read More
Company:Siemens Medical Solutions USA, Inc.Date of Enforcement Report 2/14/2018 Class lI: PRODUCT Syngo.plaza systems with SW VB20A, Model Number – 10863171, 10863172, 10863173Product Usage:Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning....
Read More
Company:Philips Medical Systems (Cleveland) Inc Date of Enforcement Report 2/14/2018 Class lI: PRODUCT Philips Ingenuity CT computed tomography x-ray system Recall Number Z-0521-2018 REASON Numerous issues related to software Brilliance iCT 4.1.6 software version. RECALLING FIRM/MANUFACTURER Philips Medical Systems (Cleveland) Inc, Cleveland, OH on 10/6/2017. Voluntary: Firm Initiated recall is ongoing. VOLUME OF PRODUCT IN...
Read More
Company:Roche Diagnostics CorporationDate of Enforcement Report 2/7/2018 Class lI: PRODUCT Roche / Hitachi MODULAR Analyzer Systems-Immunoassay Analyzer-Model/Catalog/Part Number: 11568248001/11568248692 – Elecsys 2010 analyzer (disk system) and 11804014001/11804014692 – Elecsys 2010 analyzer (rack system) Medical Device Listing number: D053244 – Elecsys 2010 Elecsys analyzer is a fully automated, random access, computer controlled analytical systems for quantitative...
Read More
Company:Edwards Lifesciences, LLCDate of Enforcement Report 27/2018 Class lI: PRODUCT Hemosphere System with the following three components: HEM1 Advanced Monitor, HEMSGM10 (Swan-Ganz Module), and HEMOXSC100 (Oximetry Smart Cable). Product Usage: The HemoSphere Advanced Monitor (HEM1) is intended to be used in combination with a compatible Edwards hemodynamic monitoring technology module and/or cable and accompanying Edwards...
Read More
Company:Roche Diagnostics CorporationDate of Enforcement Report 2/7/2018 Class lI: PRODUCT cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number: 04775279001/04775279973 – cobas e 411 analyzer (disk system) and 04775201001/04775201973 – cobas e 411 analyzer (rack system), medial device listing number: E116019 cobas e 411 Elecsys analyzer is a fully automated, random access, computer controlled analytical systems for quantitative...
Read More
Company:Carl Zeiss Metrology IncDate of Enforcement Report 2/7/2018 Class lI: PRODUCT Metrotom 800 (130kV CT scanner) Industrial CT scanner for measuring and inspecting complete components made of plastic or light metal. Recall Number Z-0379-2018 REASON Due to a software error, it was observed that when the user closes the access door, the system will resume...
Read More
Company:Siemens Medical Solutions USA, Inc.Date of Enforcement Report 2/7/2018 Class lI: PRODUCT Syngo.plaza Picture Archiving and Communication System (PACS) with software version VB20A; Model numbers: 10863171, 10863172, 10863173Syngo.plaza is a Picture Archiving and Communication System (PACS) software device intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the...
Read More
Company:GE Medical Systems Information Technologies, Inc.Date of Enforcement Report 27/2018 Class lI: PRODUCT GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2The CARESCAPE Central Station is intended to collect information from a network and display this data. This data includes physiological, patient demographic and/or other non-medical information Recall Number Z-0487-2018 REASON CARESCAPE Central Station (CSCS)...
Read More
Company:Philips Medical Systems (Cleveland) IncDate of Enforcement Report 1/31/2018 Class lI: PRODUCT Brilliance iCT – Model 728306 Computed Tomography X-ray systems Recall Number Z-0403-2018 REASON Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect scan start position, data acquisition, exam stop, tube overheat, memory overflow, failure to give error message, length of acquisition, image...
Read More
Company:Medtronic Inc., Cardiac Rhythm and Heart FailureDate of Enforcement Report 1/31/2018 Class lI: PRODUCT MyCareLink Patient Monitors. It is intended for used with a compatible Medtronic patient implanted heart device. The monitor is an external electronic device that interfaces with Medtronic implanted heart devices and a telecommunications connection to transmit stored implanted heart device data...
Read More
Company:Siemens Medical Solutions USA, Inc.Date of Enforcement Report 1/31/2018 Class lI: PRODUCT Syngo Imaging version V31 (model # 10014063) is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images, including digital mammography images. It supports the physician in diagnosis and treatment planning. Recall...
Read More
Company:Philips Medical Systems (Cleveland) IncDate of Enforcement Report 1/31/2018 Class lI: PRODUCT Brilliance iCT SP – Model 728311 Brilliance iCT – Model 728306 Computed Tomography X-ray systems Recall Number Z-0402-2018 REASON Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect scan start position, data acquisition, exam stop, tube overheat, memory overflow, failure to give...
Read More
Company:Medtronic Inc., Cardiac Rhythm and Heart FailureDate of Enforcement Report 1/31/2018 Class lI: PRODUCT MyCareLink Smart Patient Monitors. It is intended for use with a compatible Medtronic patient implanted heart device. The reader is a portable electronic device that communicates with an implanted heart device Recall Number Z-0400-2018 REASON Patients monitored on two (2) or...
Read More
Company:Phadia US Inc.Date of Enforcement Report 1/24/2018 Class lI: PRODUCT Phadia 1000 Instrument, Article Number 12-3800-01.. Recall Number Z-0387-2018 REASON The “Retry” command does not function properly which could cause a shortage of Wash and Rinse solution and affect assay performance and test results RECALLING FIRM/MANUFACTURER Phadia US Inc, Portage, MI. on 7/5/2017. Voluntary firm...
Read More
Company:RAYSEARCH LABORATORIES AB. Date of Enforcement Report 1/24/2018 Class lI: PRODUCT RayStation Product Usage: is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose distributions expected during the proposed treatment, and may be used to administer treatments after review and...
Read More
Company:OrthoScan IncDate of Enforcement Report 1/17/2018 Class lI: PRODUCT Mobile Mini C-arm system Part # 1000-0001. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.. Recall Number Z-0258-2018 to Z-0261-2018 REASON OrthoScan Inc. discovered during investigation of a...
Read More
Company:Invivo CorporationDate of Enforcement Report 12/27/2017 Class lI: PRODUCT Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when non-invasive indicators warrant such.. Recall Number Z-0263-2018 REASON Beckman Coulter has identified that due to a software nonconformity in connection with a changed service setting Remisol could display wrong results....
Read More
Company:Ortho-Clinical DiagnosticsDate of Enforcement Report 12/20/2017 Class lI: PRODUCT enGen Track System with TCAutomation Software Version 4.2 Recall Number Z-0254-2018 REASON A software anomaly with TCA Software V4.2 may potentially cause a delay in reporting of results due to patient samples being routed to an unintended location when samples are reintroduced back onto the enGEN...
Read More
Company:Normand InformatiqueDate of Enforcement Report 12/20/2017 Class lI: PRODUCT Remisol Advance Software (Driver Architect) Catalog Number B32129 The Remisol Advance Data Manager (Stand alone Data Management Systems) collects and manages data and manages workflows for connected systems. (i.e. Beckman Coulter Instruments, Automations, LIS &). It provides data analysis capabilities such as automatic results validation, delta...
Read More
Company:Radiometer America Date of Enforcement Report 12/20/2017 Class lI: PRODUCT ABL800 analyzer with FLEXQ module.Device intended for in vitro testing of samples of whole blood for the parameters pCO2, cK+, cNa+, cCa2+, cCl , cGlu, cLac, cCrea, ctBil, and co-oximetry parameters (ctHb, sO2, and the hemoglobin fractions FO2Hb, FCOHb, FMetHb, FHHb and FHbF) – in...
Read More
On Dec. 14, 2017, the FDA released a Draft guidance dated Dec. 15, 2017 “The Least Burdensome Provisions: Concept and Principles.” This guidance discusses FDA’s intent and approach to applying Least Burdensome Principles to the total product lifecycle for medical devices based on requirements in FDAMA (Public Law 105-115), the FDA Safety and Innovation Act...
Read More
Company:GE Medical Systems Information Technologies, Inc.Date of Enforcement Report 12/13/2017 Class lI: PRODUCT CARESCAPE Patient Data Module (PDM) v2.6 software used with CARESCAPE Monitors B850, B650, and B450 v2.0.7 or earlier softwareThe PDM is intended to provide uninterrupted acquisition of physiologic parameter data on adult, pediatric and neonatal patients during non-transport/bedside and transport patient care...
Read More
Company:ICU Medical IncDate of Enforcement Report 12/13/2017 Class lI: PRODUCT ICU Mednet(TM) Medication Management Suite 6.1 and 6.21, Product Code/List Numbers:(a) 16037-64-01; MedNet 6.1b) 16037-64-02; MedNet 6.1c) 16037-64-03; MedNet 6.1d) 16037-64-04; MedNet 6.21The ICU Medical MedNet Medication Management Suite (MMS) is intended to facilitate networked communication between MMS compatible computer systems and MedNet compatible infusion...
Read More
Company:Roche Diabetes Care, Inc.Date of Enforcement Report 12/13/2017 Class lI: PRODUCT Accu-Chek Connect diabetes management software app, Catalog number 07562462001 / GTIN number 00365702700000, Catalog number 07250452001 / GTIN number 00365702700017 The Accu-Chek Connect Diabetes Management App is indicated as an aid in the treatment of diabetes. The software provides for electronic download of blood...
Read More
On Dec. 8, 2017, the FDA released the draft guidance, “Clinical and Patient Decision Support Software.” This guidance addresses software for decision support in two categories: one used by Healthcare Professionals, the other used personally by patients and non-health professionals. It provides FDA interpretation of which types of Decision Support Software do not meet the...
Read More
On Dec. 8, 2017, the FDA released the final guidance, “Software as a Medical Device (SAMD): Clinical Evaluation.” The October 14, 2016, draft is now obsolete. This guidance is actually the use of an International Medical Device Regulators Forum (IMDRF) document completed in June of 2017, so this represents broad international consensus. This guidance discusses...
Read More
On Dec. 8, 2017, the FDA released draft guidance, “Changes to Existing Medical Software Policies Resulting from Section 3060 of the 21st Century Cures Act.” This guidance discusses software functions in relation to the modified device definition in the 21st Century Cures Act and the criteria for interpreting if and how medical software will or...
Read More
Company:Zimmer Biomet, IncDate of Enforcement Report 12/6/2017 Class lI: PRODUCT ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional...
Read More
Company:BRAINLAB AGDate of Enforcement Report 12/6/2017 Class lI: PRODUCT BRAINLAB EXACTRAC VERO, Model/Catalog Numbers: 46228 EXACTRAC VERO 3.5 46238 EXACTRAC VERO 3.5 46216 EXACTRAC VERO SW UPDATE 3.5.2 TO 3.5.3 46218 EXACTRAC VERO SW UPDATE 3.5.3 TO 3.5.4 The ExacTrac Vero system is intended to be used in conjunction with the MHI-TM2000 Radiation Therapy Linear...
Read More
Company:Zimmer Biomet, IncDate of Enforcement Report 12/6/2017 Class lI: PRODUCT Rosa Spine 1.0.2 Stereotaxic Instrument Computer-Assisted Surgical Device The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by surgeons to guide standard neurosurgical instruments during spine surgery. Recall Number Z-0177-2018 REASON A design change was...
Read More
Company:Volcano Corp.Date of Enforcement Report 12/6/2017 Class lI: PRODUCT Volcano Imaging System s5i REF 807400001; CORE Mobile Imaging System (120V) REF 400-0100.01; CORE Mobile Imaging System Refurbished REF 400-0100.01-R; CORE Mobile Imaging System (240V) REF 400-0100.07; CORE Mobile Imaging System Refurbished REF 400-0100.07-R; CORE Mobile Imaging System (100V) REF 400-0100.08; CORE Mobile Imaging System Refurbished...
Read More
Company:Zimmer Biomet, IncDate of Enforcement Report 11/29/2017 Class lI: PRODUCT ROSA Surgical Device 2.5.8. Recall Number Z-0115-2018 REASON Potential for software to change the final tool orientation for the command position without command. RECALLING FIRM/MANUFACTURER Zimmer Biomet, Inc.Warsaw, IN on 4/8/2016. Voluntary firm initiated recall is complete. VOLUME OF PRODUCT IN COMMERCE 64 units DISTRIBUTION...
Read More
Company:Spacelabs Healthcare, Ltd.Date of Enforcement Report 11/29/2017 Class l: PRODUCT Arkon Anesthesia Delivery System, Model 99999, and software version 2.61 and upgrade kit 050-9043-00 Rev G. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of oxygen, air and nitrous oxide...
Read More
Company:3M Company – Health Care BusinessDate of Enforcement Report 11/29/2017 Class lI: PRODUCT 3M Bair Hugger(TM) Normothermia System, Temperature Monitoring System Sensors Model 360 (Part Number 36000) Recall Number Z-0114-2018 REASON During a recent investigation, 3M confirmed that a programming translation error could occur in a small amount of the sensors that could lead to...
Read More
CompanySiemens Medical Solutions USA, IncDate of Enforcement Report 11/29/2017 Class lI: PRODUCT Syngo.plaza, Picture Archiving and Communications System(PACS), Model 10863171 Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. Recall Number Z-0168-2018 REASON Siemens is releasing a non-medical software application LTA...
Read More
Company:Zimmer Biomet, IncDate of Enforcement Report 11/22/2017 Class lI: PRODUCT ROSA Surgical Device 2.5.8. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Recall Number Z-0102-2018 REASON An undetected shift between the information displayed in the navigation software and the actual...
Read More
Company:Siemens Medical Solutions USA, Inc..Date of Enforcement Report 11/22/2017 Class lI: PRODUCT Symbia Intevo 16, SPECT/CT System, Emission Computed Tomography System To detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588keV. Serial Number: 2136,...
Read More
Company:Siemens Medical Solutions USA, Inc..Date of Enforcement Report 11/22/2017 Class lI: PRODUCT Symbia Intevo 6, SPECT/CT System, Emission Computed Tomography System To detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588keV. Serial Number: 2141,...
Read More
Company:ICU Medical IncDate of Enforcement Report 11/22/2017 Class lI: PRODUCT Plum 360 Infusion System, List number 30010. Recall Number Z-0101-2018 REASON (1) Under certain conditions, if a malfunction alarm occurs while the pump is in the “Paused” state waiting for the distal pressure to decrease, the pump cannot be turned off and delivery cannot be...
Read More
Want a free Android app as a quick reference to the regulations? Paul Felten of SoftwareCPR has developed a new app just for that purpose. You can find it by searching for “SoftwareCPR” in the Google Play store!  Google Play – SoftwareCPR app
Read More
The FDA issued its first approval of a Digital Medicine, ABILIFY MYCITE®, a new innovative treatment option in mental health. Otsuka, with the help of Proteus Inc., developed a sensor as part of the pill that communicates externally to provide confirmation the pill was ingested, along with details about it. This is for serious mental...
Read More
Company:Boston Scientific Corporation.Date of Enforcement Report 11/15/2017 Class lI: PRODUCT RESONATE EL ICD VR, Model D432, Sterile. Recall Number Z-0077-2018 REASON The devices have an incorrect firmware configuration. RECALLING FIRM/MANUFACTURER Boston Scientific Corporation, Saint Paul, MN. on 10/4/2017. Voluntary: Firm Initiated recall is complete. VOLUME OF PRODUCT IN COMMERCE 5 devices DISTRIBUTION The devices were...
Read More
Company:Biosense Webster, Inc.Date of Enforcement Report 11/8/2017 Class lI: PRODUCT THERMOCOOL SMARTTOUCH Bi-Directional Navigation Catheter (D-132704-S, D-132705-S) Recall Number Z-0056-2018 REASON Biosense Webster, Inc. has recently received an increased number of complaints related to the display of Alert 402 on the CARTO 3 System for certain lots of THERMOCOOL brand catheters. Alert 402 implies a...
Read More
Company:Biosense Webster, Inc.Date of Enforcement Report 11/8/2017 Class lI: PRODUCT THERMOCOOL SMARTTOUCH SF Bi-Directional Product Codes D-1348-01-S, D-1348-04-S, D-1348-05-S Recall Number Z-0055-2018 REASON Biosense Webster, Inc. has recently received an increased number of complaints related to the display of Alert 402 on the CARTO 3 System for certain lots of THERMOCOOL brand catheters. Alert 402...
Read More
1 3 4 5 6 7 59

SoftwareCPR Training Courses:

Being Agile & Yet Compliant (Public)

Our SoftwareCPR unique approach to incorporating agile and lean engineering to your medical device software process training course is now open for registration!

  • Agile principles that align well with medical
  • Backlog management
  • Agile risk management
  • Incremental and iterative software development lifecycle management
  •  Frequent release management
  • And more!

3 days virtual (Zoom) with group exercises, quizzes, examples, Q&A.

Lead Instructor: Mike Russell

Next public offering: Dec 3, 4, & 5, 2024 – 12:00 pm to 5:00 pm CET

Register Now


 

IEC 62304 and other emerging standards for Medical Device and HealthIT Software

Our flagship course for preparing regulatory, quality, engineering, operations, and others for the activities and documentation expected for IEC 62304 conformance and for FDA expectations. The goal is to educate on the intent and purpose so that the participants are able to make informed decisions in the future.  Focus is not simply what the standard says, but what is meant and discuss examples and approaches one might implement to comply.  Special deep discount pricing available to FDA attendees and other regulators.

3-days onsite with group exercises, quizzes, examples, Q&A.

Instructor: Brian Pate

Next public offering:  TBD

Call or email now to schedule a private, in-house class. The fall schedule is filling up!

Email training@softwarecpr.com to request a special pre-registration discount.  Limited number of pre-registration coupons.

Registration Link:

TBD

 


 

Medical Device Cybersecurity (Public or Private)

This course takes a deep dive into the US FDA expectations for cybersecurity activities in the product development process with central focus on the cybersecurity risk analysis process. Overall approach will be tied to relevant standards and FDA guidance documentation. The course will follow the ISO 14971:2019 framework for overall structure but utilize IEC 62304, IEC 81001-5-1, and AAMI TIR57 for specific details regarding cybersecurity planning, risk characterization, threat modeling, and control strategies.

2-days onsite with group exercises, quizzes, examples, Q&A.

Instructor: Dr Peter Rech, 2nd instructor (optional)

Next public offering:  TBD

Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.