Stryker Medical Division of Stryker Corporation - Class 2 Recall
Michael Graves with Stryker Highback Chair-intended for pediatric and adult person guest and patient seating use in an indoor medical setting, Model Number 4853, Part #4853000000 ¿ (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 7, 2021 Category: Medical Devices Source Type: alerts
Stryker Medical Division of Stryker Corporation - Class 2 Recall
CUB Pediatric Crib- intended to provide a pediatric patient support surface for medical purposes and to provide a method of transporting pediatric patients within a healthcare facility Model Number: FL19 Part #5050000000 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 7, 2021 Category: Medical Devices Source Type: alerts
GE OEC Medical Systems, Inc - OEC 3D - Class 2 Recall
OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic and digital spot images of adult and pediatric populations during diagnostic, interventional, and surgical procedures (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 30, 2021 Category: Medical Devices Source Type: alerts
Mediana Co., Ltd. - Vital Signs Monitor - Class 2 Recall
AVSM3 SNF, Vital Signs Monitor The monitor is intended to be used to monitor noninvasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), pulse rate (PR), temperature (Temp) for adult, pediatric and neonatal patients in all areas of a hospital and hospital-type facilities. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 20, 2021 Category: Medical Devices Source Type: alerts
Philips Respironics, Inc. - DreamStation, DreamStation Go, Dorma 400, Dorma 500, and REMstar SE Auto - Class 1 Recall
SystemOne (Q-Series), DreamStation, DreamStation Go, Dorma 400, Dorma 500, REMstar SE Auto Noncontinuous Ventilators The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for individuals with Respiratory Insufficiency. It is specifically for the care of adult and pediatric patients >7 years of age and >18kgs. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 14, 2021 Category: Medical Devices Source Type: alerts
Philips Respironics, Inc. - DreamStation ASV, DreamStation ST, AVAPS, SystemOne ASV4, CSeries ASV, CSeries S/T and AVAPS, Omni - Class 1 Recall
DreamStation ASV, DreamStation ST, AVAPS, SystemOne ASV4, C-Series ASV, C-Series S/T and AVAPS, OmniLab Advanced+ Continuous Ventilator, Non-life Supporting The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for individuals with Respiratory Insufficiency. It is specifically for the care of adult and pediatric patients >7 years of age and >18kgs. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 14, 2021 Category: Medical Devices Source Type: alerts
Philips Respironics, Inc. - Philips Respironics E30 with Humidifier - Class 1 Recall
Philips Respironics E30 with Humidifier, Continuous Ventilator, Minimum Ventilatory Support, Facility Use; Product Numbers DSX9999H11, INX9999H19, RINX9999H19 The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for individuals with Respiratory Insufficiency. It is specifically for the care of adult and pediatric patients >7 years of age and >18kgs. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 14, 2021 Category: Medical Devices Source Type: alerts
SPINEART SA - PERLA TL Lateral Connector Open - Class 2 Recall
PERLA TL Lateral Connector Open - Product Usage: intended to be used with autograft and/or allograft. Pediatric pedicle screw fixation is limited to a posterior approach. Models: PERLA TL Lateral Connector Open, 15mm PERLA TL Lateral Connector Open, 30mm (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 29, 2021 Category: Medical Devices Source Type: alerts
Covidien, LP - AdultPediatric Electrostatic Filter HME - Class 2 Recall
Adult-Pediatric Electrostatic Filter HME, Item Code 352/5877Z - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 17, 2021 Category: Medical Devices Source Type: alerts
Philips North America Llc - IntelliVue MX40 Patient Monitor - Class 2 Recall
IntelliVue MX40 Patient Monitor, Model Number: 865350 (US) 865352 (OUS) Software version number B.06.59 - Product Usage: Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and during transport inside hospitals. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 22, 2021 Category: Medical Devices Source Type: alerts
D-VITE PEDIATRIC ORAL LIQUID (cholecalciferol) solution [Akron Pharma]
Updated Date: Fri, 14 May 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 14, 2021 Category: Drugs & Pharmacology Source Type: alerts
TRI-VITE PEDIATRIC ORAL SOLUTION (vitamin a palmitate, sodium ascorbate, cholecalciferol) solution [Akron Pharma]
Updated Date: Fri, 14 May 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 14, 2021 Category: Drugs & Pharmacology Source Type: alerts
POLY-VITE PEDIATRIC ORAL SOLUTION (vitamin a palmitate, sodium ascorbate, cholecalciferol, alpha-tocopherol acetate,thiamine hydrochloride, riboflavin 5-phosphate sodium, niacinamide, pyridoxine hydrochloride, cyanocobalamin) solution [Akron Pharma]
Updated Date: Fri, 14 May 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 14, 2021 Category: Drugs & Pharmacology Source Type: alerts
D-VITE PEDIATRIC ORAL LIQUID (cholecalciferol) solution [Akron Pharma]
Updated Date: Tue, 11 May 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 11, 2021 Category: Drugs & Pharmacology Source Type: alerts
Siemens Medical Solutions USA, Inc - AXIOM ARTIS MODULAR ANGIOGRAPHIC SYSTEM; Artis Zee/Zeego & Artis Q/Q.Zen - Class 2 Recall
Artis systems - Product Usage: an angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Model Numbers: System Material # AXIOM Artis FC 05904433; AXIOM Artis FA 05904441; AXIOM Artis MP 05904466; AXIOM Artis BC 05904649; AXIOM Artis BA 05904656; AXIOM Artis dBC Mag. Nav. 05917054; AXIOM Artis TA 07007755; AXIOM Artis dTA 07008605; AXIOM Artis dFC 07412807; AXIOM Artis dTC 07413078; AXIOM Artis dBA 07555357; AXIOM Artis dMP 07555365; AXIOM Artis dFA 07555373; AXIOM Artis dFC Mag. Nav. 07727717; AXIOM Artis TC...
Source: Medical Device Recalls - April 27, 2021 Category: Medical Devices Source Type: alerts
