566 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Recall
×
BacT/ALERT FN Culture Bottles, Product Number 259793
FDA Recall
Terminated
·bioMerieux, Inc.·Product code MBD·February 16, 2007
(1) BD Pyxis MedStation ES, Catalog No. 323; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) BD Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis MedStation 4000 Console, Catalog No. 309; (5) BD Pyxis MedStation 4000, Catalog No. 303; (6) BD Pyxis Anesthesia System 4000, Catalog No. 338
FDA Recall
Open, Classified
·CareFusion 303, Inc.·Product code BRY·January 8, 2025
BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JQP·March 9, 2022
Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460
FDA Recall
Open, Classified
·Davol, Inc.·Product code FTL·April 25, 2023
Ventralight ST 4.5" Circle with Echo PS- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of soft tissue deficiencies during laparoscopic ventral hernia repair. Catalog Number: 5955450
FDA Recall
Open, Classified
·Davol, Inc.·Product code FTL·April 25, 2023
BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software version 5.1 and 5.1.1 as part of the Icefall A platform. An in vitro diagnostic medical device intended to automate specimen processing according to user-defined procedures and protocols. Catalog (Ref) No. : 447213
FDA Recall
Open, Classified
·Becton Dickinson & Co.·Product code JTC·March 22, 2023
BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample collection using evacuated BD Vacutainer Blood or Urine Collection Tubes Catalog Number: 364902, 36490200
FDA Recall
Open, Classified
·Becton Dickinson & Company·Product code JKA·January 6, 2022
Ventralight ST w EchoPS 4"x6" Ellipse- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of soft tissue deficiencies during laparoscopic ventral hernia repair. Catalog Number: 5955460G (EU Only)
FDA Recall
Open, Classified
·Davol, Inc.·Product code FTL·April 25, 2023
BD Synapsys Informatics Solution, Catalog Number 444150
FDA Recall
Open, Classified
·Becton Dickinson & Co.·Product code JQP·June 8, 2023
Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of soft tissue deficiencies during laparoscopic ventral hernia repair. Catalog Number: 5955450G (EU only)
FDA Recall
Open, Classified
·Davol, Inc.·Product code FTL·April 25, 2023
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829570, UDI: (01) 00801741027192 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code LJT·March 25, 2021
BD Alaris Pump Module REF 8100 The BD Alaris System with Guardrails Suite MX is a modular infusion pump and monitoring system for the continuous or intermittent administration of fluids to adult, pediatric, and neonatal patients through clinically accepted routes of administration
FDA Recall
Open, Classified
·CareFusion 303, Inc.·Product code FRN·January 23, 2025
BD Synapsys Informatics Solution with software versions: 4.20, 4.30, 5.10, 5.20 and 5.30- IVD standalone laboratory software solution providing data management and workflow management functionality across locations where clinical diagnostic activities take place. Catalog Number: 444150
FDA Recall
Open, Classified
·Becton Dickinson & Co.·Product code JQP·September 12, 2024
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829500, UDI: (01) 00801741027185 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code LJT·March 25, 2021
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 5829502, UDI: (01)00801741027406 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code LJT·March 25, 2021
BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
FDA Recall
Open, Classified
·Becton Dickinson & Co.·Product code LON·September 23, 2025
BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.
FDA Recall
Open, Classified
·Becton Dickinson & Co.·Product code OZN·September 23, 2025
Bone Marrow Aspiration Kit, consists of 3 main components packaged in a box. 1. Marrow Loc (Bone Marrow Specimen Acquisition System), 2. "J" Style Bone Marrow Biopsy Needle (11g (3.0mm)x10cm (4.0)) 3. BD 20ml Syringe.
FDA Recall
Terminated
·Theken Spine LLC·Product code KNW·August 27, 2008
BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument Top Remanufactured Bactec Fx, Catalog Number: 441676. 3. BACTEC 9240 System, Catalog Number: 445569. 4. BD BACTEC FX40 Instrument, Catalog Number: 44229609.
FDA Recall
Open, Classified
·Becton Dickinson & Co.·Product code MDB·September 23, 2025
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
FDA Recall
Open, Classified
·CareFusion 303, Inc.·Product code PHC·February 18, 2025