257 results · 63ms · Sources: EU EUDAMED, US FDA

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Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are intended for single use only. L Providence Medical Technology, Inc. 3875 Hopyard Road, Suite 300, Pleasanton, CA 94588, Rx Only.

FDA Recall
Terminated ·PROVIDENCE MEDICAL TECHNOLOGIES·Product code HWC·March 29, 2019

Horizon Cardiology Hemo Monitoring System A programmable diagnostic computer intended for acquiring digitizing, storing, displaying , and reviewing hemodynamic data for use in hospital cardiac catherization laboratories.

FDA Recall
Terminated ·McKesson Provider Technologies Medical Imaging Group·Product code DQK·January 27, 2010

Horizon Cardiology ECG Management This is a software application designed for use in various hospital departments to import, display, store, analyze, distribute, and process ECG procedures from resting ECG devices. It is also intended to provide analysis or reanalysis or testings ECGs and to provide preliminary data for editing and confirmation by an over-reading physician. Horizon Cardiology ECG Management may provide a serial comparison of ECG Data to facilitate the review of the patient's current ECG with previous ECG's of the same patient.

FDA Recall
Terminated ·McKesson Provider Technologies Medical Imaging Group·Product code DQK·June 16, 2010

Horizon Cardiology Hemo Component Schiller Argus Pro PB-1000 Monitor unit. Argus Pro PB 1000 firmware versions 2.41+M NIBP and 2.42.01+M. A programmable diagnostic computer intended for acquiring, digitizing, storing, displaying and reviewing hemodynamic data for use in hospital cardiac catheterization laboratories. The system is cleared for us with a component physiological data collection unit - the Schiller Argus Pro PB 1000 Monitor unit.

FDA Recall
Terminated ·McKesson Provider Technologies Medical Imaging Group·Product code DQK·April 15, 2010

Pyxis Anesthesia System 3500, Cardinal Health, Clinical Technologies and Services, San Diego, CA. The Pyxis Anesthesia Station 3500 is a medication dispensing product that provides medication and inventory management for the anesthesiologist at the point of care within the operating room. The system tracks and stores controlled substances, medications and supplies for anesthesia providers and automates verification of patient usage records, documents waste, manages inventory levels and tracks utilization.

FDA Recall
Terminated ·Cardinal Health Manufacturing LLC·Product code BRY·December 24, 2008

Blom-Singer Adjustable Tracheostoma Valve II Models: BE8025H and BE8025H-R3

FDA Recall
Terminated ·Helix Medical LLC·Product code EWL·October 1, 2013

Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product Description: 11-0494 - ICEMAN CLASSIC CUBE The IceMan CLASSIC3 cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan helps provide extended cold therapy to aid in a variety of indications and protocols as directed by a medical professional. The IceMan CLASSIC3 utilizes DonJoy's recirculation technology. Component: no

FDA Recall
Open, Classified ·DJO, LLC·Product code ILO·March 19, 2026

JK Bariatric Beds, True Air Technologies, Inc.

FDA Recall
Terminated ·SCM True Air Technologies LLC·Product code OSI·March 18, 2014

ECATS E 850 Bariatric Bed, True Air Technologies, Inc.

FDA Recall
Terminated ·SCM True Air Technologies LLC·Product code OSI·March 18, 2014

MaXair True Low Air Loss Mattress Replacement System, True Air Technologies, Inc.

FDA Recall
Terminated ·SCM True Air Technologies LLC·Product code FNM·March 18, 2014

Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,RH Model/Catalog Number: 11-1422 Software Version: no Product Description: 11-1422 - ICEMAN W/,UNIV,LOOP,NS,RH The IceMan CLASSIC3 cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan helps provide extended cold therapy to aid in a variety of indications and protocols as directed by a medical professional. The IceMan CLASSIC3 utilizes DonJoy's recirculation technology. Component: No

FDA Recall
Open, Classified ·DJO, LLC·Product code ILO·March 19, 2026

Brand Name: DONJOY Product Name: ICEMAN, W/COLDPAD, NS, RH Model/Catalog Number: 11-9099 Software Version: No Product Description: 11-9099 - ICEMAN, W/COLDPAD, NS, RH The IceMan CLASSIC3 cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan helps provide extended cold therapy to aid in a variety of indications and protocols as directed by a medical professional. The IceMan CLASSIC3 utilizes DonJoy's recirculation technology. Component: No

FDA Recall
Open, Classified ·DJO, LLC·Product code ILO·March 19, 2026

Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Product Description: 11-1424 - ICEMAN W/,UNIV,LOOP,NS,EH The IceMan CLASSIC3 cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan helps provide extended cold therapy to aid in a variety of indications and protocols as directed by a medical professional. The IceMan CLASSIC3 utilizes DonJoy's recirculation technology. Component: No

FDA Recall
Open, Classified ·DJO, LLC·Product code ILO·March 19, 2026

Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Infuser RI-2. Designed to be used in general operation in hospital or alternate care environments to provide warmed blood and fluids to any patients e10 kg requiring warmed infusion. Part Number:903-00006

FDA Recall
Open, Classified ·Belmont Instrument LLC·Product code FRN·January 2, 2025

Angiotech, T-Lok Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. The device is intended for use during Bone Marrow Biopsy.

FDA Recall
Terminated ·Medical Device Technologies, Inc.·Product code KNW·July 16, 2008

Angiotech, Bone Marrow Aspiration Needle, Medical Device Technologies, Inc. Individual packaged in blister pack. Packaged 10 per box. Sterile.

FDA Recall
Terminated ·Medical Device Technologies, Inc.·Product code KNW·July 16, 2008

Angiotech, Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. The device is intended for use during Bone Marrow Biopsy.

FDA Recall
Terminated ·Medical Device Technologies, Inc.·Product code KNW·July 16, 2008

Angiotech, Bone Marrow Harvest Needle, Medical Device Technologies, Inc. The device is intended for use Bone Marrow Biopsy.

FDA Recall
Terminated ·Medical Device Technologies, Inc.·Product code KNW·July 16, 2008

Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is t protect equipment from contamination during a variety of procedures throughout the clinical setting.

FDA Recall
Terminated ·Blue Belt Technologies MN·Product code KKX·July 19, 2013

CritiCool, thermoregulation device

FDA Recall
Open, Classified ·Belmont Instrument Corporation·Product code DWJ·July 20, 2021