Riverpoint Medical, LLC - Velosorb Fast Braided Absorbable Suture - Class 2 Recall
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 6/0 VL 18" P-10, Product Number: SV32, UDI: 20884521153117 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2020 Category: Medical Devices Source Type: alerts
Riverpoint Medical, LLC - Velosorb Fast Braided Absorbable Suture - Class 2 Recall
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 18" P-12 Cutting SV497G, UDI: 20884521149707 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2020 Category: Medical Devices Source Type: alerts
Riverpoint Medical, LLC - Velosorb Fast Braided Absorbable Suture - Class 2 Recall
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" KV-15 TaperCutting CV2279, UDI: 20884521151632 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2020 Category: Medical Devices Source Type: alerts
Riverpoint Medical, LLC - Velosorb Fast Braided Absorbable Suture - Class 2 Recall
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 5/0 Undyed 30" KV-11, TaperCutting, Product Number: CV2293, UDI: 20884521151588 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2020 Category: Medical Devices Source Type: alerts
Riverpoint Medical, LLC - Velosorb Fast Braided Absorbable Suture - Class 2 Recall
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18" P-12 Cut, Product Number: SV496, UDI: 20884521184258 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2020 Category: Medical Devices Source Type: alerts
Riverpoint Medical, LLC - Velosorb Fast Braided Absorbable Suture - Class 2 Recall
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18" PC-10, Product Number: SV835G, UDI: 20884521149721 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular Us Sales, Llc - ROTAFLOW Centrifugal Pump System - Class 3 Recall
Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) - Product Usage: Instructions for Use - Centrifugal Pump System is a device that uses a method other than revolving rollers to pump the blood through an extracorporeal circuit Material Number: 701043292 (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 12, 2020 Category: Medical Devices Source Type: alerts
Terumo Cardiovascular Systems Corporation - Terumo Advanced Perfusion System 1 - Class 2 Recall
Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32, Catalog Number 5791 - Product Usage: intended for use with Terumo and Sarns brand air detection and heart-lung systems to detect gross air bubbles in the line during extracorporeal procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 12, 2020 Category: Medical Devices Source Type: alerts
Terumo Cardiovascular Systems Corporation - Terumo Advanced Perfusion System 1 - Class 2 Recall
Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32, Catalog Number 5773 - Product Usage: intended for use with Terumo and Sarns brand air detection and heart-lung systems to detect gross air bubbles in the line during extracorporeal procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 12, 2020 Category: Medical Devices Source Type: alerts
Terumo Cardiovascular Systems Corporation - Terumo Advanced Perfusion System 1 - Class 2 Recall
Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK, Catalog Number 5785 - Product Usage: intended for use with Terumo and Sarns brand air detection and heart-lung systems to detect gross air bubbles in the line during extracorporeal procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 12, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular Us Sales, Llc - Holder HKHZ 19 for use with Quadroxi and QuadroxiD Neonatal / Pediatric Oxygenators - Class 2 Recall
Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal / Pediatric Oxygenators, Model Number: 701047495 - Product Usage: The Holder HKHZ 19 is an accessory to QUADROX i and QUADROX iD Neonatal / Pediatric oxygenator and is being used as a single holder for QUADROX i and QUADROX iD Neonatal / Pediatric Oxygenator and can also be used in combination with the holder's arm (016061) to use in cardiopulmonary bypass procedures (CPB) in a pediatric patient population. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 13, 2020 Category: Medical Devices Source Type: alerts
Merge Healthcare, Inc. - VERICIS CARDIOVASCULAR IMAGE AND INFORMATION SYSTEM, MODEL 4.0 - Class 2 Recall
Merge Healthcare Merge Application Server Software Release and Merge Healthcare Merge Cardio Workstation Software Release - Product Usage: VERICIS is a system intended to be used to acquire, store, print, transfer, and archive clinical information from Camtronics and other vendors systems including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical character recognition of measurements captured on images) and cardiology signal (waveform) data. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 20, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - NonMagnetic Chest Pneumograph Toshiba KSB - Class 2 Recall
Cardiovascular Monitoring Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration bellows, or respiration sensor) monitors bellows-derived respiration by detecting abdominal or chest wall motion. The chest pneumograph is an accessory to a MRI patient monitoring system or MRI gating solution. The Chest Pneumograph is indicated for use by healthcare professionals with the Wireless Sp02 (wSp02) Module or Toshiba KSB gating unit when bellows-derived respiration sensing is needed during MRI scans for gating. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 3, 2020 Category: Medical Devices Source Type: alerts
Stryker Sustainability Solutions - Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter - Class 2 Recall
Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm, Sterile EO, Rx Only, Quantity 1, UDI: 07613327376067 (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 2, 2020 Category: Medical Devices Source Type: alerts
Applied Medical Resources Corp - Vascular Clip - Class 2 Recall
STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 16, 2020 Category: Medical Devices Source Type: alerts
