226 results · 23ms · 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.

NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System, Product Code HH9006, containing 6 Single-Procedure Kits (Product Code HH9001), each containing the sterile drape (HH2000), as well as single-use drug components, Manufactured for and Distributed by Novadaq Technologies Inc., Burnaby, BC, Canada, Assembled by Carestream Health, Inc., Rochester, NY. The SPY-PHI Drape is intended to cover the SPY-PHI System to maintain a sterile field, and as an aid in the clean-up of equipment after surgery or other medical procedures. The product is not intended to be used as patient drapes and they have no patient contact.

FDA Enforcement
Class II ·Terminated·NOVADAQ TECHNOLOGIES INC.·October 4, 2017

Sterile Drape, SK6000 PAQ drape pouch (for use with the SPY Fluorescent System (SPY 2000/2001)) The SPY Fluorescent Imaging System is intended to provide fluorescent images for the visual assessment of blood flow in vessels and related tissue perfusion during cardiovascular surgical procedures. For use in intraoperative visual assessment of the coronary vasculature and bypass grafts during coronary artery bypass (BABG) surgery.

FDA Enforcement
Class II ·Terminated·NOVADAQ TECHNOLOGIES INC.·September 14, 2016

Surface Applicator Set with Leipzig-style Cone. Brachytherapy applicator set.

FDA Enforcement
Class II ·Terminated·Varian Medical Systems Inc·July 1, 2015

The VariSource iX series afterloader systems are computer controlled remote electro/mechanical systems used for medical purposes, for placing a cable incorporating an irradiated iridium seed internally or close by a malignant tumor or tumor bed in a practice known as brachytherapy.

FDA Enforcement
Class II ·Terminated·Varian Medical Systems Inc·July 8, 2015

Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml EMP160ECO-US-5 (GTIN:5060358120367) Product Usage: Tissue Retrieval sac made from ripstop nylon. The EMP160ECO-US-5 is a semi-automatic sac, which incorporates a monofilament drawstring around the mouth of the bag, so that it can be pulled closed and removed from the body cavity.

FDA Recall
Terminated ·Espiner Medical Ltd Yeo Bank 3, Kenn Road Clevedon United Kingdom·Product code GCJ·June 20, 2018

Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml EMP160ECO-US-5 (GTIN:5060358120367) Product Usage: Tissue Retrieval sac made from ripstop nylon. The EMP160ECO-US-5 is a semi-automatic sac, which incorporates a monofilament drawstring around the mouth of the bag, so that it can be pulled closed and removed from the body cavity.

FDA Enforcement
Class II ·Terminated·Espiner Medical Ltd·November 21, 2018

Sterile Drape, SK6000 PAQ drape pouch (for use with the SPY Fluorescent System (SPY 2000/2001)) The SPY Fluorescent Imaging System is intended to provide fluorescent images for the visual assessment of blood flow in vessels and related tissue perfusion during cardiovascular surgical procedures. For use in intraoperative visual assessment of the coronary vasculature and bypass grafts during coronary artery bypass (BABG) surgery.

FDA Recall
Terminated ·NOVADAQ TECHNOLOGIES INC.·Product code IZI·August 18, 2016

The Gyrus ACMI Pleatman Sac Tissue Removal System facilitates removal of specimens while minimizing contamination of the abdominal cavity or wound tract. The system contains one (1) Sac and one (1) obturator in a sterile, ready -to -use, single- use procedure tray.

FDA Recall
Terminated ·Gyrus Acmi, Incorporated·Product code GCJ·August 3, 2010

DLP(R) Pericardial/Intracardiac Sump Cannulae, 20 Fr., P/N: 12112. This product is intended for draining the pericardial sac or the cardiac chambers.

FDA Recall
Terminated ·Medtronic Cardiovascular Revascularization & Surgical Therap·Product code DWF·September 29, 2008

The Guardian Connect App CSS7200 iOS - Product Usage: intended for use by patients with a compatible consumer mobile device.

FDA Recall
Terminated ·Medtronic Inc.·Product code MDS·July 15, 2020

ReadyMed Elastomeric Ambulatory Pump, Model Numbers: R050050, R100100, R100200, R250050, R250100, and R250167. Intended for self-administration of anti-microbial and antiviral agents.

FDA Recall
Terminated ·Cardinal Health 303 dba Cardinal Health·Product code FRN·December 19, 2008

Freedom Designs TriPod w/Anti tipper Manual Wheelchair, Models Numbers: TriPod, Tripod LT and TriPod Pediatric LT with Trailing Anti-Tipper-Caster-Axle Link, Freedom Designs Incorporated, Simi Valley, CA 93065

FDA Recall
Terminated ·Freedom Designs Inc·Product code IOR·May 14, 2007

MiniMed 620G Insulin Infusion Pump, Catalog No. MMT-1510, MMT-1710, MMT-1550, MMT-1750.

FDA Recall
Terminated ·Medtronic Inc.·Product code OZO·May 8, 2017

MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.

FDA Recall
Terminated ·Medtronic Inc.·Product code OZP·May 8, 2017

MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.

FDA Recall
Terminated ·Medtronic Inc.·Product code OZO·May 8, 2017

MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752.

FDA Recall
Terminated ·Medtronic Inc.·Product code OZP·May 8, 2017

Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 55, Catalog Number LG-PR0855, Allez Spine, LLC., Irvine, CA

FDA Recall
Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 80, Catalog Number LG-PR0880, Allez Spine, LLC., Irvine, CA

FDA Recall
Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 45, Catalog Number LG-PR0845, Allez Spine, LLC., Irvine, CA

FDA Recall
Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 35, Catalog Number LG-PR0835, Allez Spine, LLC., Irvine, CA

FDA Recall
Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007