Angiodynamics Inc. (Navilyst Medical Inc.) - BioFlo Port with ENDEXO and PASV Valve Technology - Class 2 Recall
XCELA, 8F SINGLE PLASTIC PORT FILLED, VALVED, UPN H965440400, Cat. No. 44-040 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2019 Category: Medical Devices Source Type: alerts
Angiodynamics Inc. (Navilyst Medical Inc.) - BioFlo Port with ENDEXO and PASV Valve Technology - Class 2 Recall
BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVED, UPN H965440210, Cat. No. 44-021 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2019 Category: Medical Devices Source Type: alerts
Angiodynamics Inc. (Navilyst Medical Inc.) - BioFlo Port with ENDEXO and PASV Valve Technology - Class 2 Recall
BIOFLO 8F SINGLE TITANIUM NON- FILLED; VALVED, UPN H965440250, Cat. No. 44-025 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2019 Category: Medical Devices Source Type: alerts
Angiodynamics Inc. (Navilyst Medical Inc.) - BioFlo Port with ENDEXO and PASV Valve Technology - Class 2 Recall
BIOFLO 8F SINGLE PLASTIC FILLED; NON-VALVED, UPN H965440140, Cat. No. 44-014 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2019 Category: Medical Devices Source Type: alerts
Fenwal Inc - VOLUMAT MC AGILIA US - Class 1 Recall
VOLUMAT MC AGILIA US, Infusion Pump, REF Z021135, software versions 1.7 and 1.9a Product Usage: The Volumat MC Agilia is a piece of transportable medical equipment intended to be used in healthcare facilities environment by healthcare trained professionals according to hospital protocols on adults, pediatrics and neonatal human patient to administer via a single channel or mounted on a multiple channels rack accessory: Intermittent or continuous delivery of parenteral fluids (solutions, colloids, parenteral nutrition) and medications (including but limited to diluted drugs, chemotherapy) through clinically accepted IV ro...
Source: Medical Device Recalls - August 13, 2019 Category: Medical Devices Source Type: alerts
Cardinal Health 200, LLC - ChemoPlus Chemo Spill Kit - Class 2 Recall
ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 7, 2019 Category: Medical Devices Source Type: alerts
Cardinal Health 200, LLC - ChemoPlus Chemo Spill Kit - Class 2 Recall
ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 7, 2019 Category: Medical Devices Source Type: alerts
Cardinal Health 200, LLC - ChemoPlus Protective Wraparound Goggles - Class 2 Recall
ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 7, 2019 Category: Medical Devices Source Type: alerts
Cardinal Health 200, LLC - ChemoPlus Chemo Spill Kit - Class 2 Recall
ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 7, 2019 Category: Medical Devices Source Type: alerts
Elekta, Inc. - MOSAIQ Oncology Information System and Sequencer - Class 2 Recall
MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be used wherever radiotherapy and/or chemotherapy are prescribed. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 9, 2019 Category: Medical Devices Source Type: alerts
Arrow International Inc - Arrow CVC - Class 2 Recall
Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm, Reference # CS-12402 The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access, including, but not limited to the following: " Lack of usable peripheral IV sites " Central venous pressure monitoring " Total parenteral nutrition (TPN) " Infusions of fluids, medications, or chemotherapy " Frequent blood sampling or receiving blood transfusions/blood products (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 12, 2019 Category: Medical Devices Source Type: alerts
Fresenius Vial Sa - Volumat MC Agilia - Class 2 Recall
Volumat MC Agilia Volumetric Infusion Pump, Model No. Z021135, Software version 1.7. Product Usage - The Volumat MC Agilia is a piece of transportable medical equipment intended to be used in healthcare facilities environment by healthcare trained professionals according to hospital protocols on adults, pediatrics and neonatal human patient to administer via a single channel or mounted on a multiple channels rack accessory: Intermittent or continuous delivery of parenteral fluids (solutions, colloids, parenteral nutrition) and medications (including but limited to diluted drugs, chemotherapy) through clinically accepted IV...
Source: Medical Device Recalls - November 2, 2018 Category: Medical Devices Source Type: alerts
Arrow International Inc - ARROWgard Blue Plus MultiLumen CVC Kit - Class 2 Recall
Arrow AGB + Multi-Lumen CVC Kit, Cat. No. CDC-42703-B1A. Product Usage - The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access, including, but not limited to the following: Lack of usable peripheral IV sites, Central venous pressure monitoring, Total parenteral nutrition (TPN), Infusions of fluids, medications, or chemotherapy, and Frequent blood sampling or receiving blood transfusions/blood products. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 27, 2018 Category: Medical Devices Source Type: alerts
Angiodynamics Inc. (Navilyst Medical Inc.) - BioFlo Port with ENDEXO and PASV Technology - Class 2 Recall
BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVED PG UPN: H965440210 Catalog Number: 44-021 Box of 1 Port - Product Usage - Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 6, 2018 Category: Medical Devices Source Type: alerts
Arrow International Inc - Pressure Injectable Multi - Class 2 Recall
Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to: multiple infusions of fluids, medications, or chemotherapy infusion of fluids that are hypertonic, hyperosmolar, or have divergent pH values frequent blood sampling or blood/blood component infusions infusion of incompatible medications central venous pressure monitoring lack of usable peripheral ...
Source: Medical Device Recalls - March 15, 2018 Category: Medical Devices Source Type: alerts
