344 results
·
14ms
·
Sources: EU EUDAMED, US FDA
MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";
FDA Recall
Open, Classified
·Aesculap Inc·Product code HCF·December 29, 2023
Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: 70845357041233 Product Usage: On April 9, 2019, Microbiologics sent ACTION REQUIRED: MEDICAL DEVICE CORRECTION emails to their direct US consignees requesting them to complete a MEDICAL DEVICE CORRECTION FORM indicating how much product they had on hand.
FDA Recall
Open, Classified
·Microbiologics Inc·Product code PMN·April 9, 2019
Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019, Microbiologics sent ACTION REQUIRED: MEDICAL DEVICE CORRECTION emails to their direct US consignees requesting them to complete a MEDICAL DEVICE CORRECTION FORM indicating how much product they had on hand.
FDA Recall
Open, Classified
·Microbiologics Inc·Product code PMN·April 9, 2019
Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories. Philips Respironics V60 Ventilator Part Number U1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories. Note: U1053617 added 1/29/2021 after noticing it had been inadvertently left off
FDA Recall
Open, Classified
·Respironics California, LLC·Product code MNT·November 2, 2020
Mojo Full Face with Headgear, All Sizes
FDA Recall
Open, Classified
·SleepNet Corporation·Product code BZD·March 1, 2024
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.
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code BZD·June 14, 2021
Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZD·April 20, 2023
DreamStation Auto BiPAP. Non-Continuous Ventilator.
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code BZD·June 30, 2025
HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZD·April 20, 2023
Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZD·April 20, 2023
Phantom 2 Nasal Vented Mask
FDA Recall
Open, Classified
·SleepNet Corporation·Product code BZD·March 1, 2024
Philips Respironics DreamWear Full Face Mask
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code BZD·September 6, 2022
Therapy Mask 3100 NC/SP
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code BZD·September 6, 2022
AirTouch F20 Full Face Mask and User Guide
FDA Recall
Open, Classified
·Product code BZD·November 20, 2023
Mojo 2 Full Face AAV Non Vented Mask, All Sizes
FDA Recall
Open, Classified
·SleepNet Corporation·Product code BZD·March 1, 2024
iQ 2 Nasal Vented Mask
FDA Recall
Open, Classified
·SleepNet Corporation·Product code BZD·March 1, 2024
DreamStation Auto CPAP. Non-Continuous Ventilator.
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code BZD·June 30, 2025
Mojo 2 Full Face Vented Mask, All Sizes
FDA Recall
Open, Classified
·SleepNet Corporation·Product code BZD·March 1, 2024
Mojo 2 Full Face Non Vented Mask, All Sizes
FDA Recall
Open, Classified
·SleepNet Corporation·Product code BZD·March 1, 2024
DreamWisp Nasal Mask with Over the Nose Cushion
FDA Recall
Open, Classified
·Philips Respironics, Inc.·Product code BZD·September 6, 2022