44 results · 21ms · 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.

Material CVI2590, INSERTION/PPE KIT, CENTURION INSERTION/PPE KIT, Reorder CVI2590, CENTURION MEDICAL PRODUCTS CORP. WILLIAMSTON MI 48895 USA 800.248.4058 www.centurionmp.com, LATEX FREE STERILE FACILITATES LINE PLACEMENT

FDA Recall
Terminated ·Centurion Medical Products Corporation·Product code LRS·March 31, 2011

Centurion Medical Products Insertion/PPE Kit CV12590, Sterile.

FDA Recall
Terminated ·Centurion Medical Products·Product code LRS·June 2, 2010

MSI-EpiDermGlu (Iso-Butyl 2 Cyanoacrylate) tissue adhesive for soft tissue approximation; 0.22 cc plastic squeeze tubes packaged in a Tyvek/PPE pouch with paper label, 10 units per case; Manufactured by Medisav Services Inc. (MSI), 56 Elson Street, Markham, Ontario L3S 1Y7 Canada

FDA Recall
Terminated ·Elite Medical Group·Product code MPN--·July 3, 2003

Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340 (GTIN #816329023404); 5341 (GTIN #816329023411); 5342 (GTIN #816329023428); 5343 (GTIN #816329023435) - Product Usage: General Hospital Use

FDA Recall
Terminated ·Cadence Science, Inc.·Product code FMF·May 10, 2019

Alkaline Wash, List number 9D31-20, a cleaning solution used by the Abbott Architect analyzers. It is supplied in 500 mL bottles and contains NaOCl, NaOH, and KOH. It is shipped and stored at room temperature and is shipped ready to use.

FDA Recall
Terminated ·Abbott Laboratories·Product code JJE·May 11, 2015

Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during cardiopulmonary bypass (CPB) or similar procedures with extracorporeal circulation, which require continuous monitoring of the arterial and/or venous blood parameters: partial pressure of oxygen (pO2), temperature (TArt and TVen), oxygen saturation (SO2), hemoglobin (Hb) and hematocrit (Hct).

FDA Recall
Terminated ·Maquet Cardiovascular Us Sales, Llc·Product code DRY·September 30, 2020

Artificial ligament fixation device # 7PE ZIPLOOP Extended Toggle, Sterile, REF 904755, Biomet Sports Medicine Warsaw, IN. Intended for soft tissue to bone fixation.

FDA Recall
Terminated ·Biomet, Inc.·Product code MBI·March 31, 2010

ToggleLoc; fastener, fixation, non degradable, soft tissue; Artificial Ligament Fixation Device #7 PE Ziploop Extended Toggleloc Product Usage: The Toggleloc System is a non-resorbable system intended to aid in arthroscopic and orthopedic reconstructive procedures requiring soft tissue fixation, due to injury or degenerative disease.

FDA Recall
Terminated ·Biomet, Inc.·Product code JDR·February 26, 2015

KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged into 3 oz tubes, which are then packed into a printed carton. Distributed by McNeil-PPC Inc.

FDA Recall
Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·January 25, 2013

KY LIQUIBEADS Vaginal Moisturizer; Distributed By: McNeil-PPC, Inc. Skillman, NJ 08558-9418; UPC 380041087704; 380040087958. Personal lubricant

FDA Recall
Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·July 2, 2012

KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is packaged in 2.5 oz bottles, which are then packed into a printed carton. Distributed by McNeil-PPC Inc.

FDA Recall
Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·January 25, 2013

KY TINGLING JELLY Personal Lubricant. The product is packaged into 5 oz tubes with the UPC printed on it. Distributed By: McNeil-PPC Inc.

FDA Recall
Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·January 25, 2013

Artificial Ligament Fixation Device 15MM TI NS ToggleLoc (TM) W/Continuous Maxbraid Polyethylene Suture Loop TO Gal 4V Alloy/Polyethylene; Artificial Ligament Fixation Device 25MM TI NS ToggleLoc (TM) W/Continuous Maxbraid Polyethylene Suture Loop TO Gal 4V Alloy/Polyethylene; Artificial Ligament Fixation Device 20MM TI NS ToggleLoc (TM) W/Continuous Maxbraid Polyethylene Suture Loop TO Gal 4V Alloy/Polyethylene; Artificial Ligament Fixation Device 30MM TI NS ToggleLoc (TM) W/Continuous Maxbraid Polyethylene Suture Loop TO Gal 4V Alloy/Polyethylene; Artificial Ligament Fixation Device 35MM TI NS ToggleLoc (TM) W/Continuous Maxbraid Polyethylene Suture Loop TO Gal 4V Alloy/Polyethylene; Artificial Ligament Fixation Device #7 PE Ziploop (TM) ToggleLoc (TM). Toggleloc anchors are indicated for use for fixation of tendons & ligaments during orthopedic reconstruction procedures such as Anterior Cruciate Ligament (ACL) reconstruction.

FDA Recall
Terminated ·Biomet Sports Medicine·Product code MBI·April 24, 2008

MEDICREA LIGAPASS TENSION PULLEY HANDLE XS- intended to provide thoracic and/or lumbar posterior stabilization for degenerative pathologies Ref : A08200200

FDA Recall
Terminated ·Medicrea International Vancia Vancia Rillieux La Pape France·Product code OWI·October 8, 2020

Exacta Mix TPN (total parenteral nutrition) Bag, Model 740, 2000mL, Baxa Corporation

FDA Recall
Terminated ·Baxa Corporation·Product code KPE·November 12, 2009

EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set.

FDA Recall
Terminated ·Baxter Healthcare Corporation·Product code KPE·September 12, 2018

EXACTAMIX Empty EVA Bags - 2000 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set.

FDA Recall
Terminated ·Baxter Healthcare Corporation·Product code KPE·September 12, 2018

Exacta Mix TPN (total parenteral nutrition) Bag, Model 738, 500mL, Baxa Corporation.

FDA Recall
Terminated ·Baxa Corporation·Product code KPE·November 12, 2009

Exacta-Mix Calibration Bag, Sterile R, non-pyrogenic fluid path, 250 mL Reorder No. H938 371 3, Manufactured for Baxa Corporation.

FDA Recall
Terminated ·Baxa Corporation·Product code KPE·May 26, 2010

Exacta-Mix 2400 Valve Assembly w/Calibration Bag, Sterile R, 250 mL, Order No. REF: 724, Baxa Corporation.

FDA Recall
Terminated ·Baxa Corporation·Product code KPE·May 26, 2010