By

Amy Sellers
Company:NordicNeuroLab AS Date of Enforcement Report 6/6/2018 Class lI: PRODUCT nordicBrainEXProduct Usage:nordicBrainEx is an image processing software package to be used by trained professionals including but not limited to physicians and medical technicians. The software runs on a standard off-the-shelf PC workstation and can be used to perform image viewing, processing and analysis of medical...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/30/2018 Class lI: PRODUCT Biograph Horizon, PET/CT System using VJ10A, VJ10B, VJ20A scanners that provide registration and fusion of high resolution physiologic and anatomic information.SOMATOM Force (Model 10742326) Computed tomography x-ray diagnostic system Recall Number: Z-1930-2018 REASON Possibility that the Biograph Horizon systems performing CT retrospective...
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Company:Baxter Healthcare CorporationDate of Enforcement Report 5/30/2018 Class lI: PRODUCT Prismaflex System, Product Code 107493 Intended Use: The Prismaflex Control Unit is intended for: ” Continuous Renal Replacement Therapy (CRRT) for patients weighing 20 kilograms or more with acute renal failure and/or fluid overload. ” Therapeutic Plasma Exchange (TPE) therapy for patients weighing 20 kilograms...
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Company:Baxter Healthcare CorporationDate of Enforcement Report 5/30/2018 Class lI: PRODUCT Prismaflex 7.XX ROW, Product Code 114870: The Prismaflex Control Unit is intended for: ” Continuous Renal Replacement Therapy (CRRT) for patients weighing 20 kilograms or more with acute renal failure and/or fluid overload. ” Therapeutic Plasma Exchange (TPE) therapy for patients weighing 20 kilograms or...
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Company:Baxter Healthcare CorporationDate of Enforcement Report 5/30/2018 Class lI: PRODUCT Prismaflex 7.20 US: The Prismaflex Control Unit is intended for: ” Continuous Renal Replacement Therapy (CRRT) for patients weighing 20 kilograms or more with acute renal failure and/or fluid overload. ” Therapeutic Plasma Exchange (TPE) therapy for patients weighing 20 kilograms or more with diseases...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/23/2018 Class lI: PRODUCT SOMATOM Force (Model 10742326) Computed tomography x-ray diagnostic system Recall Number: Z-1748-2018 REASON There is a potential risk of unnecessary radiation exposure due to a software issue found in the CARE Dose4D algorithm implemented in Siemens Healthineers CT scanners of types SOMATOM...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/23/2018 Class lI: PRODUCT SOMATOM Definition AS (Model 8098027) Computed tomography x-ray diagnostic system Recall Number: Z-1745-2018 REASON There is a potential risk of unnecessary radiation exposure due to a software issue found in the CARE Dose4D algorithm implemented in Siemens Healthineers CT scanners of types...
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Company:Invivo Corporation Date of Enforcement Report 5/23/2018 Class lI: PRODUCT PHILIPS Xper Flex Cardio Physiomonitoring System, Model Numbers: 453564241901, 453564483321, 453564621791, and 989803199561 (international only)The Xper Flex Cardio physiomonitoring system is used to facilitate invasive investigation of heart and vascular, disease when non-invasive indicators warrant such. Recall Number: Z-1867-2018 REASON The real-time numeric value for...
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Company:Draegar Medical Systems, Inc. Date of Enforcement Report 5/23/2018 Class lI: PRODUCT Infinity Acute Care System (lACS) Monitoring Solution; Catalog Numbers:MS20401, MS20724, MS22956, MS25510, MS25520, MS25643, MS26196, MS26372, MS31818; UDI Information: 4049098054454, 4049098054447, 4049098054409, 4049098009799, 4049098009751. Multi-parameter, physiologic patient monitoring of adult, pediatric and neonatal patients in environments where patient care is provided by trained...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/16/2018 Class lI: PRODUCT Syngo.plaza software VB10A model numbers: 10863171, 10863172, 10863173 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. Syngo.plaza also...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/16/2018 Class lI: PRODUCT Syngo.plaza software 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. Syngo.plaza also supports storage and archiving of DICOM...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/16/2018 Class lI: PRODUCT ACUSON SC2000 Ultrasound System. The firm name on the label is Siemens Medical Solutions USA, Inc., Buffalo Grove, IL.. Recall Number: Z-1200-2018 REASON The ECG signal may flatline due to electromagnetic interference during the use of electrosurgical equipment. RECALLING FIRM/MANUFACTURER Siemens Medical...
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Company:Inpeco S.A. Date of Enforcement Report 5/16/2018 Class lI: PRODUCT FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System Recall Number: Z-1798-2018 REASON Module may freeze without generating user warning. There is a potential risk in delay of sample processing, leading to delayed delivery of test results to patients RECALLING FIRM/MANUFACTURER Inpeco S.A....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Sensation 10 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1453-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Spirit Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1451-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior)...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Sensation Open Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1457-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Sensation Emotion Duo (2003) Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1459-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Sensation Cardiac Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1455-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Sensation 64 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1456-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Sensation 40 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1458-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Sensation 16 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1454-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Scope Power Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1450-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Scope Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1449-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior)...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Perspective 16 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1448-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Emotion 6 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1445-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Emotion 16 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1446-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Emotion (2003) Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1452-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Perspective Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1447-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior)...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT Biograph Horizon – PET/CT, PETsyngo VJ20A Software Nuclear medicine/ xray diagnostic scanner. Recall Number: Z-15972018 REASON Error introduced into PET images acquired and reconstructed with VJ20A software. Array values are indexed improperly when the norm file is created during QC. During data...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 5/9/2018 Class lI: PRODUCT SOMATOM Perspective 16 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data. Recall Number: Z-1448-2018 REASON To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a....
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Company:Philips Electronics North America Corporation Date of Enforcement Report 5/9/2018 Class lI: PRODUCT Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray system Product Usage: The Allura Xper ED series is intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional...
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Company:PerkinElmer Life and Analytical Sciences, Wallac, OYDate of Enforcement Report 5/9/2018 Class lI: PRODUCT Specimen Gate Screening Center, Part Number 5002-0500, All software versions from 1.0 to 1.8 (current software version) Specimen Gate Screening Center is used for data management of neonatal screening test results and demographics by qualified laboratory personnel in newborn screening programs....
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Company:Hitachi Ltd., Medical System Operations Group Date of Enforcement Report 5/9/2018 Class lI: PRODUCT MHI-TM2000 Linear Accelerator System Product Usage: MHI-TM2000 Linear Accelerator System is intended for radiation therapy of lesions, tumors and conditions anywhere in the body where radiation treatment is indicated. Recall Number: Z-1585-2018 REASON Due to a system controller software anomaly, the...
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Company:Roche Diagnostics CorporationDate of Enforcement Report 5/9/2018 Class lI: PRODUCT cobas b 221Roche OMNI S2 system catalog numbers: 3337111001 and 3337111692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, urea/BUN, total...
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Company:Roche Diagnostics CorporationDate of Enforcement Report 5/9/2018 Class lI: PRODUCT cobas b 221Roche OMNI S2 system catalog numbers: 3337111001 and 3337111692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, urea/BUN, total...
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Company:Roche Diagnostics CorporationDate of Enforcement Report 5/9/2018 Class lI: PRODUCT cobas b 221Roche OMNI S2 system catalog numbers: 3337111001 and 3337111692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, urea/BUN, total...
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Company:Radiometer Medical ApSDate of Enforcement Report 5/9/2018 Class lI: PRODUCT AQURE, Software version 2.3.0 and 2.3.1 Product Usage: The AQURE system is intended to let allow the management of analytical devices and operator profiles. The user can associate patient data with test data. The system shows test results. The system receives data from connected devices...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 4/25/2018 Class lI: PRODUCT PRIMUS HI, Digital Linear Accelerator, Model No. 07360717 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer Recall Number: Z-1402-2018 REASON Control Console software has been updated to reduce the risk for collision...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 4/25/2018 Class lI: PRODUCT ONCOR Impression, Digital Linear Accelerator, Model No. 07360717 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer Recall Number: Z-1400-2018 REASON Control Console software has been updated to reduce the risk for collision...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 4/25/2018 Class lI: PRODUCT ONCOR Impression plus, Digital Linear Accelerator, Model No. 07360717 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer Recall Number: Z-1401-2018 REASON Control Console software has been updated to reduce the risk for...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 4/25/2018 Class lI: PRODUCT ONCOR Expression, Digital Linear Accelerator, Model No. 07360717 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer Recall Number: Z-1399-2018 REASON Control Console software has been updated to reduce the risk for collision...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 4/25/2018 Class lI: PRODUCT ONCOR Avant-garde, Digital Linear Accelerator, Model No. 05863472 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer. Recall Number: Z-1398-2018 REASON Control Console software has been updated to reduce the risk for collision...
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Company:Siemens Medical Solutions USA, Inc Date of Enforcement Report 4/25/2018 Class lI: PRODUCT MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer. Recall Number: Z-1397-2018 REASON Control Console software has been updated to reduce the...
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Company:Philips Medical Systems (Cleveland) IncDate of Enforcement Report 4/25/2018 Class lI: PRODUCT ngenuity TF PET/CT, Model No. 882442 Product Usage: The device is an integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) system suitable for a wide range of diagnostic applications. The device utilizes the CT technology to obtain anatomic images of...
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Company:GE Medical Systems Ultrasound & Primary Care Diagnostics, Date of Enforcement Report 4/25/2018 Class lI: PRODUCT GE Healthcare:a) Prodigy, Model Numbers: LU7248, LU8905, LU40427, LU40431, LU40626, LU40637, LU40626, LU40637, LU42021, LU42025, LU41730, LU41734, LU42344, LU42365 b) Prodigy Advanced, Model Numbers: LU42361, LU42397Provides an estimate of BMD (Bone Marrow Density) at the lumbar spine and proximal...
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Company:GE Medical Systems Ultrasound & Primary Care Diagnostics, Date of Enforcement Report 4/25/2018 Class lI: PRODUCT 1. GE Healthcare Lunar: a) DPX Duo, Model Number: LU41693 b) DPX Bravo, Model Number: LU41692 Provides an estimate of BMD (Bone Marrow Density) at the lumbar spine and proximal femur regions. This BMD value can then be compared...
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Company:Beckman Coulter Inc.Date of Enforcement Report 4/18/2018 Class lI: PRODUCT iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100. Recall Number Z-1366-2018 REASON iQ200 Series Urine Microscopy Analyzer may intermittently fail to read urine sample dilution barcode labels causing erroneous results that could delay treatment for health conditions such as hematuria. RECALLING FIRM/MANUFACTURER Beckman...
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Company:Beckman Coulter Inc.Date of Enforcement Report 4/18/2018 Class lI: PRODUCT BECKMAN COULTER iQ200 Series Urine Microscopy Analyzer Recall Number Z-1362-2018 REASON Beckman Coulter has determined that there is a potential for under-reporting casts. This can occur if per high-power field (/HPF) units of measurement for casts are selected in the iQ200 software, but the abnormal...
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Company:Philips Electronics North America CorporationDate of Enforcement Report 4/18/2018 Class lI: PRODUCT IntelliVue X3 Patient Monitor.. Recall Number Z-1315-2018 REASON The NBP measurement of Intellivue X3 Patient Monitor shows intermittently only mean values instead of the diastolic and systolic blood pressure values. This is caused by a falsely detected NBP cuff, which is leading to...
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Company:Lifeline Systems Company.Date of Enforcement Report 4/18/2018 Class lI: PRODUCT HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator. Recall Number Z-1316-2018 REASON A programing error in some Model FD100 HomeSafe AutoAlert Pendants will render the fall detection feature inoperable. RECALLING FIRM/MANUFACTURER Lifeline Systems Company, Framingham, MA on 11/13/2017. Voluntary: Firm Initiated recall...
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