BEUDAMED
    40 results · 14ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Recall × Status: Terminated × Clear all

    Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to provide an aesthetically pleasing design that will enhance the overall experience for the bariatric patient. Using spring box construction and an exceptionally smooth mechanism, the patient is able to move into a reclined position with little effort and infinite positions up to 38 degrees. An independent footrest enables patients to be in a fully seated position with their feet up for added comfort.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code FRJ·January 20, 2016

    HeartStart FR2+ Defibrillator

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·December 19, 2006

    HeartStart FR2+ AED with ECG Display, Model 3840, Laerdal brand, configurable manual charge in advance mode. The label of the device states: "HEARTSTART...FR2+ Automated External Defibrillator...Manufactured by: Philips Medical Systems Seattle, WA 98121".

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·September 22, 2010

    HeartStart FR2+ AED with Text Display (No ECG), Model M3861, Philips brand, no configurable manual charge. The label of the device states: "HEARTSTART...FR2+ Automated External Defibrillator...Manufactured by: Philips Medical Systems Seattle, WA 98121".

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·September 22, 2010

    HeartStart FR2+ AED with Text Display (No ECG), Model 3841, Laerdal brand, no configurable manual charge. The label of the device states: "HEARTSTART...FR2+ Automated External Defibrillator...Manufactured by: Philips Medical Systems Seattle, WA 98121".

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·September 22, 2010

    HeartStart FR2+ AED with ECG Display, Model M3860, Philips brand, configurable manual charge in advance mode. The label of the device states: "HEARTSTART...FR2+ Automated External Defibrillator...Manufactured by: Philips Medical Systems Seattle, WA 98121".

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·September 22, 2010

    EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-FR1

    FDA Recall
    Terminated ·Arrow International Inc·Product code CAZ·January 15, 2020

    Haylard Closed Suction System for Neonates/Pediatrics, 5 Fr, 1. REF 195, Y-Adapter, SAP Finished Product Code 109382303; 2. REF 201, with BALLARD Technology, SAP Finished Product Code 109382803; 3. REF 202, Elbow, SAP Finished Product Code 109382903; 4. REF 195-5 Y-Adapter, SAP Finished Product Code 109838302.

    FDA Recall
    Terminated ·Avanos Medical, Inc.·Product code BSY·November 5, 2019

    HeartStart FR2+ AED with Text Display, Model 989803148611. This product is G2005 Update in accordance with the American Heart Association 2005 Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care (ECC). The label of the device states: "HEARTSTART...FR2+ Automated External Defibrillator...Manufactured by: Philips Medical Systems Seattle, WA 98121".

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·September 22, 2010

    HeartStart FR2+ AED with ECG Display, Model 989803148601. This product is G2005 Update according to the American Heart Association 2005 Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care (ECC). The label of the device states: "HEARTSTART...FR2+ Automated External Defibrillator...Manufactured by: Philips Medical Systems Seattle, WA 98121".

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·September 22, 2010

    Philips HeartStart FR2+ Defibrillator Automated External Defibrillator (AED) Catalog Numbers: M3860A/M3861A/M3840A/M3841A

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·February 28, 2007

    HeartStart FR2+ automated external defibrillator (AED) Model M3860: Philips brand; configurable ECG on screen; configurable manual charge in advance mode.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·May 28, 2010

    HeartStart FR2+ automated external defibrillator (AED) model: M3840: LAERDAL brand; configurable ECG on screen; configurable manual charge in advance mode.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·May 28, 2010

    HeartStart FR2+ automated external defibrillator (AED) model: M3841: LAERDAL brand; text prompts only on screen (NO ECG); no configurable manual charge.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·May 28, 2010

    HeartStart FR2+ automated external defibrillator (AED) model: M3861: PHILIPS brand; text prompts only on screen (NO ECG); no configurable manual charge.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·May 28, 2010

    Arrow Pediatric Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter, 5 Fr., 2 Lumen, 13cm catheter length, Catalog number: CS-14502.

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·June 17, 2009

    Heartstart FR2+ automated external defibrillator Models M3860A and M3840A are equipped with an ECG Module. M3860A is under the Philips label and M3840A is under the Laerdal label.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·October 1, 2009

    Heartstart FR2+ automated external defibrillator models M3861A and M3841A are NOT equipped with the ECG Module. Model M3861A is under the Philips label and M3841A is under the Laerdal label.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·October 1, 2009

    BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System, catalog number 245000. in vitro diagnostic for the identification of aerobic gram-negative bacteria that belong to the family Enterobacteriaceae as well as some of the more frequently isolated glucose fermenting and nonfermenting gram-negative bacilli.

    FDA Recall
    Terminated ·Becton Dickinson & Co. 7 Loveton Cir BD Diagnostic Systems·Product code JSS·May 21, 2014

    27023WU Balloon Catheter, 3 Fr., 2/pkg, sterile, contains latex. The RUSCH ureter occlusion catheter is indicated for the routine occlusion of the ureter to prevent the movement of stone fragments during treatment. The coaxial catheters will also allow simultaneous drainage of urine or infusion of other solutions.

    FDA Recall
    Terminated ·Karl Storz Endoscopy America Inc·Product code GBA·May 31, 2013