123 results · 31ms · Sources: EU EUDAMED, US FDA

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Brilliance iCT model #728306; Intended to produce cross- sectional images of the body.

FDA Recall
Terminated ·Philips Medical Systems (Cleveland) Inc·Product code JAK·June 21, 2016

Ingenuity Core 128, model #728323; Intended to produce cross- sectional images of the body.

FDA Recall
Terminated ·Philips Medical Systems (Cleveland) Inc·Product code JAK·June 21, 2016

Ingenuity Flex, model # 728317; Intended to produce cross- sectional images of the body.

FDA Recall
Terminated ·Philips Medical Systems (Cleveland) Inc·Product code JAK·June 21, 2016

Ingenuity Core, model # 728326; Intended to produce cross- sectional images of the body.

FDA Recall
Terminated ·Philips Medical Systems (Cleveland) Inc·Product code JAK·June 21, 2016

Brilliance CT Big Bore Oncology, model #728243; Intended to produce cross- sectional images of the body.

FDA Recall
Terminated ·Philips Medical Systems (Cleveland) Inc·Product code JAK·June 21, 2016

Ambulance Parameter Extension (APE) kit M4758A, an accessory to the Philips HeartStart MRx Monitor/Defibrillator - Product Usage: is intended to be used with the M3536A MRx in EMS environments.

FDA Recall
Terminated ·Philips North America, LLC·Product code MKJ·January 14, 2020

Philips DigiTrak XT Holter Recorder Software version number B.1 and C.2. The DigiTrak XT Recorder is available in four different configurations. Service tag numbers for these configurations are as follows: - 453564067151 24-Hour Configuration - 453564067161 48-Hour Configuration - 453564067171 96-Hour Configuration - 453564067181 7-Day Configuration Model Number: 860322

FDA Recall
Terminated ·Philips North America, LLC·Product code MWJ·January 13, 2020

Software versions syngo.CT VB20 or VB20_SP1 in the following systems: SOMATOM Force (Model #10742326) SOMATOM Definition As (Model #8098027) SOMATOM Definition Edge (Model #10590000) SOMATOM Definition Flash (Model #10430603) SOMATOM Drive (Model #10431700) SOMATOM Confidence (Model #10590100) SOMATOM Edge Plus (Model #10267000)

FDA Recall
Terminated ·Siemens Medical Solutions USA, Inc·Product code JAK·June 22, 2020

Vereos PET/CT, Software version 2.0.1. Model Number: 882446 Product Usage: The Philips Vereos PET/CT system is a diagnostic imaging device that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem images anatomical cross-sections by computer reconstruction of X-ray transmission data. The PET subsystem images the distribution of PET anatomy-specific radiopharmaceuticals in the patient. The PET/CT system is used for the purposes of detecting, localizing, diagnosing, staging, re-staging, and follow-up for monitoring therapy response of various diseases in oncology, cardiology, and neurology. The system is intended to image the whole body, heart, brain, lung, gastrointestinal, bone, lymphatic, and other major organs for a wide range of patient types, sizes, and extent of diseases. Both subsystems can also be operated as fully functional, independent diagnostic tools, including application of the CT scanner for diagnosis and for use in radiation therapy planning.

FDA Recall
Terminated ·Philips Medical Systems (Cleveland) Inc·Product code KPS·September 4, 2018

Boston Scientific, Flexima and Percuflex Drainage Catheter Family (Pigtail Style) UPN DESCRIPTION M001271540 FLEXIMA BILIARY FIRM 8F/35CM M001271550 FLEXIMA BILIARY FIRM 10F/35CM M001271560 FLEXIMA BILIARY REG 8F/35CM M001271570 FLEXIMA BILIARY REG 10F/35CM M001271580 FLEXIMA BILIARY REG 12F/35CM M001271590 FLEXIMA BILIARY REG 14F/35CM M001271600 FLEXIMA BILIARY SOFT 10F/35CM M001271610 FLEXIMA BILIARY SOFT 12F/35CM M001271620 FLEXIMA BILIARY SOFT 14F/35CM M001281560 FLEXIMA BILIARY 8/35 TT M001281570 FLEXIMA BILIARY 10/35 TT M001281580 FLEXIMA BILIARY 12/35 TT M001281590 FLEXIMA BILIARY 14/35 TT M001271630 FLEXIMA BIL 8F/35CM FIRM KIT M001271640 FLEXIMA BIL 10F/35CM FIRM KIT M001271650 FLEXIMA BIL 8F/35CM REG KIT M001271660 FLEXIMA BIL 10F/35CM REG KIT Single Use Only, Sterilized with Ethylene Oxide Gas, Boston Scintific Corporation, One Boscton Scintific Place, Natick, MA 01760-1537, Made in USA 780 Brookside Drive, Spencer, IN 47460 1080. Designed for percutaneous drainage of abscess fluid, the Biliary system and the urinary tract.

FDA Recall
Terminated ·Boston Scientific Corporation·Product code FFA·March 18, 2009

Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using IV administration sets for continuous or intermittent delivery through clinically acceptable routes of administration such as intravenous or epidural

FDA Recall
Terminated ·CareFusion 303, Inc.·Product code FRN·December 2, 2016

QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3 QMS TACROLIMUS CAL C 10015568-3 QMS TACROLIMUS CAL D 10015569-3 QMS TACROLIMUS CAL E 10015570-3 QMS TACROLIMUS CAL F 10015571-3

FDA Recall
Open, Classified ·Microgenics Corporation·Product code MLM·January 20, 2022

AxSYM Quinidine Standard Calibrators - consist of six bottles of Cal A (6ml) and Cals B-F (4ml each)-Product List Number-7A73-01

FDA Recall
Terminated ·Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila·Product code LGI·May 31, 2007

Architect Free T4 Calibrator Kit, list 7G96-01; the kit consists of 2 bottles of calibrators, CAL 1 - 0.5 and CAL 2 - 6.0; Abbott Laboratories, Abbott Park, IL 60064

FDA Recall
Terminated ·Abbott Laboratories HPD/ADD·Product code CEC·May 30, 2003

ARCHITECT Free T4 Calibrator Kit, list 7G96-01; the kit consists of 2 bottles of calibrators, CAL 1 - 0.5 and CAL 2 - 6.0; Abbott Laboratories, Abbott Park, IL 60064

FDA Recall
Terminated ·Abbott Laboratories HPD/ADD/GPRD·Product code CEC--·December 15, 2003

Atellica CH Toxicology Calibrator (TOX CAL)-The Atellica CH Toxicology Calibrator (TOX CAL) is for in vitro diagnostic use in calibrating the Acet, ETOH and Sal assays using the Atellica CH Analyzer Siemens Material Number (SMN): 11099440

FDA Recall
Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JLX·April 5, 2023

Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number: 81557 Software Version: Not Applicable Product Description: Lumipulse G pTau 217 Plasma Calibrators: The pTau 217 plasma concentration of a specimen is automatically calculated from the calibration curve, which is also automatically calculated from calibration data. The result of the calculation is reported in pg/mL. Lumipulse G pTau 217 Plasma Calibrators: Liquid (Frozen), 1x1.5 mL (5 Concentrations) CAL 1 0 pg/mL pTau 217 Plasma Calibrator CAL 2 0.250 pg/mL pTau 217 Plasma Calibrator CAL 3 1.000 pg/mL pTau 217 Plasma Calibrator CAL 4 5.000 pg/mL pTau 217 Plasma Calibrator CAL 5 10.000 pg/mL pTau 217 Plasma Calibrator Contains Tris buffer with protein (bovine) and chemical stabilizers. Preservative: 0.1% ProClin 300, 0.05% ProClin 950 Component: Yes. Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio

FDA Recall
Open, Classified ·Fujirebio Diagnostics, Inc.·Product code SET·December 11, 2025

BIO CAL(R) Temperature Controller, Models: (a) 370, (b) 370I Product Usage: The BIO CAL(R) (unit) is a thermal transfer module designed to control patient blood temperature during cardiopulmonary bypass procedures when heating or cooling of the blood is desired.

FDA Recall
Terminated ·Medtronic Perfusion Systems·Product code DWJ·February 8, 2018

Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog Number TF10161. IVD

FDA Recall
Terminated ·Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland·Product code DDG·June 9, 2022

BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL

FDA Recall
Open, Classified ·Bio-Rad Laboratories, Inc.·Product code LIP·February 8, 2022