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Company: Intuitive Surgical, Inc., Date of Enforcement Report 2/27/2008 Class:ll PRODUCT Intuitive Surgical, daVinci S Surgical System, Model Number: IS2000, A5.1 P1 and A5.0 P5 software level, Surgical Endoscopic Instrument Control System, Model Number: IS 2000, Software Revision Numbers: A5.0 P5 and A5.1 P1, Recall # Z-0079-2008 REASON System Lock-Up: Software anomalies could cause product...
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Company: Sunquest Information Systems, Inc., Date of Enforcement Report 1/23/2008 Class:ll PRODUCT Sunquest Laboratory Blood Bank and Blood Donor Modules v6.0.1 and v6.0.2 Distributed with Sunquest Laboratory v6.1, v6.2 and v6.3 REASON In the Sunquest Blood Bank and Blood Donor Modules, a problem has been identified in Blood Product Testing. If the user chooses to...
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Company:Siemens Medical Solutions USA, Inc. Date of Enforcement Report 2/20/2008 Class:ll PRODUCT Siemans- ACUSON Aspen Diagnostic Ultrasound System, general purpose Diagnostic Ultrasound system, Model Number: 8247887, Recall # Z-0719-2008 REASON Software error: Error affects all Aspen customer systems using the PAL video standard configuration and has a Perspective PC installed. This can lead to a...
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Company: Varian Medical Systems Inc, Date of Enforcement Report 2/20/2008 Class:ll PRODUCT Varian brand VARiS 1.4g (Medical Charged Particle Radiation Therapy System, Record and Verify System); Linear Accelerator with RTP Exchange v6.2, v6.6, & v8.0, All Models, Recall # Z-0720-2008 REASON Incorrect Software Validation. The ARC treatment plans containing a Dose Dynamic MLC for IMRT...
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Company:Philips Medical Systems Date of Enforcement Report 2/20/2008 Class:ll PRODUCT Philips Medical Systems — Cardiac Viewer or Pulmonary Viewer software application version 2.0 in use with Precedence SPECT/CT System and all CT EBW workstations using software version 3.5, Recall Z-0676-2008 REASON Incorrect Measurement: The firm discovered a software defect in Cardiac and Pulmonary Viewer software...
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Company: Novartis Vaccines and Diagnostic Date of Enforcement Report 2/13/2008 Class:ll PRODUCT Procleix NAT Tracker Version 3.0 Software, Stand Alone Blood, Recall # B-0662-08 REASON Software, with a glitch or defect, was distributed. RECALLING FIRM/MANUFACTURER Novartis Vaccines and Diagnostic, Emeryville, CA, by letter on August 2, 2007 with a follow up letter on August 9,...
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Company: Sunquest Information Systems, Inc., Date of Enforcement Report 2/13/2008 Class:ll PRODUCT Sunquest Laboratory Blood Bank and Blood Donor, version 6.0.1 and 6.0.2, Recall # B-0663-08 REASON Software, with a glitch or defect, was distributed. RECALLING FIRM/MANUFACTURER Sunquest Information Systems, Inc., Tucson, AZ, by e-mail on December 14. 2007. Firm initiated recall is ongoing. VOLUME...
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Company: General Electric Medical Systems Information Technology Date of Enforcement Report 2/13/2008 Class:ll PRODUCT GE Healthcare CIC Pro Clinical Information Center, Central Station, Software Version 4.1. (CIC Pro v4.1). (System hardware consists of a processing unit and a monitor), Recall # Z-0280-2008 REASON Two separate issues may occur with operating The CiC Pro v4.1 System...
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Company: Vital Images, Inc., Date of Enforcement Report 2/6/2008 Class:ll PRODUCT Vital Images ViTALConnect, Version 4.0 and 4.1, PET/CT Visualization option. (A web-based medical diagnostic tool that allows physicians to use PCs or notebook computers to gain remote access to 2D, 3D, and 4D advanced visualization. The software enables users to measure, rotate, and analyze...
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Recipient: Spinal, USAProduct:Slimplicity Anterior Cervical Plate System, the Spinal USA Cement Restrictor and the Spinal USA Vertebral Body Replacement (VBR) System Date:12/7/2007 This inspection revealed these devices are adulterated within the meaning of Section 501(h) of the Act [21 USC 351(h)], because the methods used in, or the facilities or controls used for, their manufacture,...
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Company: Baxter Healthcare Renal Division Date of Enforcement Report 2/6/2008 Class:ll PRODUCT Baxter RenalSoft v.2.0 Patient Management Software Suite – HD Module; clinical data management software, Recall # Z-0527-2008; b) Baxter Renal Software Suite v.3.0 and v.3.1 – Renal Link HD Module; clinical data management software; Recall # Z-0528-2008 REASON Pre-Treatment/Post-Treatment Report errors: 1) The...
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Company: Varian Medical Systems, Inc., Date of Enforcement Report 2/6/2008 Class:ll PRODUCT Varian Real-Time Position Management System (RPM), A Respiratory Gating System; Version 1.7.3, All Models, Recall # Z-0554-2008 REASON Erroneously Resetting: RPM System version 1.7.3, software failure can occur that affects the gated radiotherapy treatment when phase-based gating is used. RPM 1.7 erroneously resets...
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Company: Cyberonics, Inc., , Date of Enforcement Report 2/6/2008 Class:lll PRODUCT Cyberonics, VNS Therapy System Model 250 Handheld programming system using Dell x5 handheld and preprogrammed with software v7.1 and higher, Recall # 0568-2008 REASON Screen Freezes– The Dell X5 Handheld PC screen will freeze caused due to incompatibility between the Microsoft 2002 OS and...
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Recipient:Omron Healthcare, Inc. Product:diagnostic and therapeutic foreign manufactured medical devices Date:1/18/2008 This inspection revealed, that these devices are adulterated within the meaning of Section 501(h) of the Act [21 U.S.C. 351(h)], in that the methods used in, or the facilities or controls used for, their manufacture, packing, storage, or installation are not in conformity with...
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Company: SCC Soft Computer Date of Enforcement Report 1/30/2008 Class:ll PRODUCT SoftBank II version 23.1, 23.1.1.x . , 23.1.2.x With Softscape 1.2.0.x, Recall # B-0505-08 REASON Software with a glitch or defect, was distributed. RECALLING FIRM/MANUFACTURER SCC Soft Computer, Clearwater, FL, by Task Management Notification and telephone on September 19, 2007. Firm initiated recall is...
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Company: Visx, Inc Date of Enforcement Report 1/30/2008 Class:ll PRODUCT Advanced Medical Optics (AMO), VISX WaveScan WaveFront System (software). Part Number 0070-1478, Recall # Z-0365-2008 REASON Erroneous Treatment Calculations – Two software caused errors; in combination, in the WaveScan System Software, will result in an erroneous treatment calculation (overcorrection) in patients. (1) Installation of software...
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Company: Datascope Date of Enforcement Report 1/23/2008 Class:lll PRODUCT Datascope, Panorama Patient Monitoring Network; Panorma Telepack 608; Software Versions 8.1.X, 8.3, 8.3.1, 8.4.1, and 8.5.X, Part Number: 0998-00-0191-04, Recall # Z-0150-2008 REASON Display problems: If an ECG cable, which has been damaged due to the ingress of liquid or by mechanical trauma, is utilized with...
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Dr. Nancy Leveson of MIT indicated that there are some new papers involving a demonstration of STAMP (and STPA) being used for safety-driven design of a new JPL mission to Europa including a very complete example. A JPL modeling language was incorporated (JPL was funding the work), but had little to do with the final...
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Company: Toshiba American Med Sys Inc., Date of Enforcement Report 1/16/2008 Class:ll PRODUCT Toshiba Aplio XG Diagnostic Ultrasound System, Model: SSA-790A with version 1.1 software, Recall # Z-0305-2008 REASON Panel Lock-up: When using dynamic image acquisition modes the panel may lock up, if the operator attempts to perform a still image capture. If the panel...
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Company: SCC Soft Computer Date of Enforcement Report 1/16/2008 Class:ll PRODUCT Softbank II Software Version 23.1 with database Management System Interface. Report Unique Identifier: 1058332-04/07/2006-011-C, Recall # B-0504-08 REASON Software with a glitch or defect, was distributed. RECALLING FIRM/MANUFACTURER SSCC Soft Computer, Clearwater, FL, by e-mail on May 9, 2005. Firm initiated recall is complete....
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Company: Siemens Medical Solutions USA, Inc., Date of Enforcement Report 1/16/2008 Class:ll PRODUCT a) Siemens, ACUSON Antares, Ultrasound System (Standard and Premium Edition), 5.0 Systems with software version 200.0.054, P/N: 10032747 and 10032746 standard, 10032746, 10037591, and 10038202 for premium edition, Recall # Z-0297-2008; b) Siemens, SONOLINE Antares Ultrasound System, 5.0 Systems with software version...
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http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm089402.htm
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Company: Philips Medical Systems Date of Enforcement Report 1/2/2008 Class:ll PRODUCT a) Philips Medical Systems, Cardiac Viewer or Pulmonary Viewer Application that can run on all Gemini TFs, GXLs and EBW Workstations. (The product is a software application that is installed in Philips Medical System CT scanners.), Recall # Z-0366-2008; b) Philips Medical Systems, Cardiac...
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Company: Ellex, Inc., Date of Enforcement Report 1/2/2008 Class:ll PRODUCT Ellex, Eye Cubed, I 3 System-ABD Ultrasound Version 3.0 with Software Version 3.0 and Biometry A-scan modality, Recall # Z-0148-2008 REASON Incorrect IOL calculations: software behavior with Version 3.0 Eye Cubed Ultrasound systems running Biometry A-scan enabled Version 3.0.0 software can cause incorrect IOL calculations....
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Company:Beckman Coulter Inc Date of Enforcement Report 1/2/2008 Class:ll PRODUCT a) COULTER LH750 Analyzer, Part Number: 6605632, Hematology analyzer, Recall # Z-0312-2008; b) COULTER LH780 Analyzer, Part Number: 723585, Hematology analyzer, Recall # Z-0313-2008; c) COULTER LH 500 Series System, Part Number: 178833, Hematology analyzer, Recall # Z-0314-2008; d) COULTER GEN*S System, Part Number: 6605381,...
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Company: Medtronic Navigation, Inc Date of Enforcement Report:12/26/2007 Class:lll PRODUCT Ortho Assay Software (OAS) Version 2.0.1. There is no product code for the OAS. OAS software is pre-loaded on the OAS workstation. The workstation on which the software is loaded has two product codes: Product Code 936415 – April 4, 1999 to April 24, 2007...
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Company: Data Innovations, Inc., Date of Enforcement Report:12/26/2007 Class:ll PRODUCT Data Innovations Instrument Manager Software versions 7.04.0001 through 8.04.03.01, Recall # B-0195-08 REASON Software, with a defect or glitch, was distributed. RECALLING FIRM/MANUFACTURER Data Innovations, Inc., South Burlington, VT, by e-mail on September 19, 2007 and by follow-up letter dated October 11, 2007. Firm initiated...
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Company: Philips Medical Systems Date of Enforcement Report:12/195/2007 Class:ll PRODUCT Philips Medical Systems, M3290A IntelliVue Information Center Software for M3170 Intellivue Patient Link, Catalog Number: 865007 and 865015; Running Software Versions J.00.23, J.00.24, J.00.25, and J.00.26, Recall Z-0451-2008 REASON Alarm failure: If changes are made to the Care Group Editor configuration, Care Group alarm status,...
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Company: Accuray Inc, Date of Enforcement Report:12/19/2007 Class:ll PRODUCT Accuray, Multiplan Treatment Planning Software, Recall # Z-0364-2008 REASON Software problem – Sagittal, oblique or coronal sliced MR Images imported from a non-Accuray manufactured device into the product may result in inverted image orientation. RECALLING FIRM/MANUFACTURER Accuray Inc, Sunnyvale, CA, by Urgent Advisory Notification on March...
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Company:Abbott Laboratories, Inc Date of Enforcement Report:12/19/2007 Class:ll PRODUCT a) ARCHITECT c8000 Processing Module, for In Vitro Diagnostics; List Number 106- 01; Affected software: v2.10, v2.11, v2.12, v2.20, v2.20DB, v2.30, v2.60, v3.00 and v3.10, Recall $ Z-0146-2008; b) ARCHITECT c16000 Processing Module, for In Vitro Diagnostics; List Number 3L77-01; Affected software: v2.10, v2.11, v2.12, v2.20,...
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Company: GE Healthcare Advantage WorkstationsDate of Enforcement Report:12/19/2007 Class:ll PRODUCT GE Healthcare Advantage Workstations, Advantage Workstation version 4.2 and 4.3 with Volume Viewer 2 (version 6.4-6.8) provided with Advance Vessel Analysis (AVA) and Advantage Workstation 4.4 with Volume Viewer 2 (version 6.8 or before) or Volume Viewer 3 (version 7.2 -7.3) provided with Advanced Vessel...
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https://www.softwarecpr.com/Docs/Jmurray-AAMI-Webinar-December-4-2007-A.pdf
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Brian Fitzgerald Deputy Division Director, Division of Electrical and Software Engineering, FDA CDRH, Office of Science & Engineering Laboratories, provided a list of software analysis tools FDA’s laboratory uses in evaluating medical device code. This was in response to a question posed at a recent AAMI Webinar that John Murray of FDA and Alan Kusinitz...
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Company: Medtronic Navigation, Inc Date of Enforcement Report:12/5/2007 Class:ll PRODUCT Medtronic 0-arm Imaging System, Product Catalog Number: B1-700-00027, (software version 3.0), Recall # Z-0294-2008 REASON Reversed Instrument Position: a defect in the software version 3.0 causes an error in the position of surgical instruments and relative motion are reversed 180′ on the StealthStation image. (If...
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Company:Misys Healthcare Systems Date of Enforcement Report:12.5/2007 Class:ll PRODUCT Misys Laboratory Blood Bank and Blood Donor Modules v6.0.1 and v6.0.2, Recall # B-0317-08 REASON Software, with a defect or glitch, was distributed. RECALLING FIRM/MANUFACTURER Misys Healthcare Systems dba Misys Hospital Systems, Tucson, AZ, by e-mail on August 24, 2007. Firm initiated recall is ongoing. VOLUME...
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Company:Siemens Medical Solutions USA, Inc., Date of Enforcement Report:12/5/2007 Class:ll PRODUCT a) Siemens ECAT ACCEL, Catalog No. 3545584, PET/CT Scanner, Recall # Z-0269-2008; b) Siemens ECAT ART, Catalog No.. 3545584, PET/CT Scanner, Recall # Z-0270-2008; c) Siemens ECAT EXACT 47, Catalog No. 1788772, PET/CT Scanner, Recall # Z-0271-2008; d) Siemens ECAT EXACT HR 47, Catalog...
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Company:Toshiba America Medical Systems, Inc., Date of Enforcement Report:12/5/2007 Class:ll PRODUCT Toshiba-Interventional Angiography System, Infinix i, Model DFP-8000D, equipped with Digital Radiography System with Software version 3.4er000, Recall # Z-0293-2008 REASON System Lock-up: When performing DAS One Shot, the system may lockup due to a software timing error.. RECALLING FIRM/MANUFACTURER Recalling Firm: Toshiba America Medical...
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In an AAMI Webinar John Murray of FDA indicated that it appears that software issues comprise 16 percent of medical device recalls and there is some thought to developing some special procedures for handling these. SoftwareCPR has found approximately 75 recalls related to software as of the end of November 2007 for the year which...
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Recipient:Cardinal Enterprises, Inc Product: drug products. Date: 12/1/2007 This inspection revealed significant deviations from Current Good Manufacturing Practice (cGMP) Regulations (Title 21, Code of Federal Regulations (21 “CFR), Parts 210 and 211). These deviations cause the drug products manufactured at this facility to be adulterated within the meaning of Section 501(a)(2)(B) of the Federal Food,...
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Company: Philips Medical Systems t Date of Enforcement Report:11/28/2007 Class:ll PRODUCT Philips, Voxel Q workstations, utilizing AcQSim or AcQPlan software version 4.2, 4.2.1, 4.9, 4.9.1, 4.9.2, 4.9.3, 5.0, 5.0.1, 5.0.2 or 5.0.3 and any Mx8000, Mx8001DT, or Brilliance 6, 10, 16, 16P, and Big Bore CT systems connected to the VoxelQ, Recall # Z-0180-2008 REASON...
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Company: Toshiba American Med Sys IncDate of Enforcement Report:11/21/2007 Class:ll PRODUCT a) NEMIO Ultrasound System, Model SSA-550A , Software versions: V3.1.000B, V3.5.0, V3.5.000A, V3.5.000B, V3.6.0, V3.6.000A, V4.0.0, V4.0.000A, V4.l.0, V4.l.000A, V4.2.0, V4.3.0, V4.5.0, V4.5.000A, Recall $ Z-0253-2008; b) NEMIO XG Ultrasound System, Model SSA-580A , Software versions: VI .5.0, Vl .5.000A, VI .5.000B, V2.0.0, Recall...
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Company:GE Healthcare Date of Enforcement Report:11/14/2007 Class:ll PRODUCT GE Healthcare Voluson E8 ultrasound scanner with Software version 6.2.0 and 6.2.1 and DICOM stations with these software versions; Recall # Z-0113-2008 REASON When a spectrum of a Pulsed Wave Doppler shows an angle correction unequal to 0 is reloaded from the archive or the image is...
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Company: Medtronic Inc. Cardiac Rhythm Management Date of Enforcement Report:11/14/2007 Class:lll PRODUCT Medtronic Paceart System, 2006 Edition, The Paceart System can act as a Practice Management software application and is intended for use by facilities that provide services such as event monitoring, trans-telephonic pacemaker evaluation, and in-office evaluation of implanted cardiac devices; Recall # Recall...
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Company: Philips Medical Systems (Cleveland) Inc Date of Enforcement Report:11/14/2007 Class:ll PRODUCT The Brilliance CT Big Bore is a whole body computed tomography X-Ray system. The malfunctioning software application is the Tumor Localization (Tumor LOC) application. All Brilliance CT Big Bore Scanners with Tumor Localization software versions v2.2.1, v2.2.2, & v2.2.5. This software version is...
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CENELEC decides to include 62304 harmonization for the IVD directive based on a recommendation of TC 62. This is in addition to the MDD and AIMD.
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https://www.softwarecpr.com/docs/CBERbecsvalidationguidanceDraft1007.pdf
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Company: Medtronic Neurological, Date of Enforcement Report:10/17/2007 Class:ll PRODUCT Medtronic InterStim II INS Model 3058 with N’Vision InterStim-B Software supplied on the Model 8870 Version MMB_01/NNB_01 N’Vision with a Clinican Programmer Model 8840. Implantable Neurostimulator for Urinary Control. Catalog # 8870MM01 & 8870NNB01, Recall # Z-0037-2008 REASON A software issue may cause a lower than...
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Company: Beckman Coulter Incl, Date of Enforcement Report:10/24/2007 Class:ll PRODUCT FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use. Recall # Z-0002-2008 REASON Pressure (from recapped tubes) or vacuum (from under-filled short-draw tubes) will cause inaccurate results if not properly vented. RECALLING FIRM/MANUFACTURER Recalling Firm: Beckman Coulter...
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SoftwareCPR Training Courses:

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

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

Lead Instructor: Mike Russell

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  • Americas: 11-13 February 2025
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See our post titled: 1st Quarter 2025 Agile Compliant Courses Scheduled

 

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.

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

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