47 results · 14ms · Sources: EU EUDAMED, US FDA

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Dimension Vista Prolactin (PRL) Flex reagent cartridge

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code CFT·March 21, 2017

Dimension Vista Estradiol (E2) Flex reagent cartridge

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 21, 2017

Dimension Troponin 1 (TNI) Flex reagent cartridge

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code MMI·March 21, 2017

Dimension Vista Digoxin (DIGXN) Flex reagent cartridge

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code KXT·March 21, 2017

Dimension Vista Ferritin (FERR) Flex reagent cartridge

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code DBF·March 21, 2017

Dimension Vista Thyroid Stimulating Hormone (TSH) Flex reagent cartridge

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code JLW·March 21, 2017

Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator is an in vitro diagnostic product for the calibration of follicle stimulating hormone (FSH), luteinizing hormone (LH), prolactin (PRL), and estradiol (E2) methods on the Dimension Vista System.

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code JIX·November 9, 2017

LIFESTREAM Balloon Expandable Vascular Covered Stent . BARD PERIPHERAL VASCULAR. 6mm X 26mm X 80 Recommended Introducer 6F (2.00mm) NP 8atm (811 kPa) Recommended Guide wire .035" (0.89mm) RBP 12 atm (1216 kPa) RX Only Lot numbers begins with CMA or CMB. Product Code Stent Diameter Stent length Catheter Length LSM0800626 6mm 26 mm 80 cm LSM1350626 6 mm 26 mm 135 cm LSM0800637 6 mm 37 mm 80 cm LSM1350637 6 mm 37 mm 135 cm LSM0800726 7 mm 26 mm 80 cm LSM1350726 7 mm 26 mm 135 cm Product Usage: The LIFESTREAM Balloon Expandable Vascular Covered Stent is indicated for the treatment of atherosclerotic lesions in common and external iliac arteries with reference vessel diameters between 4.5 mm and 12.0 mm, and lesions lengths up to 100mm.

FDA Recall
Terminated ·Bard Peripheral Vascular Inc·Product code PRL·February 18, 2019

Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved. Correction of varus, valgus, or posttraumatic deformity. Correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. The device is a single use implant intended for implantation with bone cement.

FDA Recall
Terminated ·Zimmer Biomet, Inc.·Product code JWH·August 9, 2016

PML --IDS Rapid NH QC Set- Quality Control kit for culture media. Product label includes LyfoCults IVD , Lot # 134-1 Exp 02AUG2008. PML Micrcobiologicals 27120 SW 95th Avenue Wilsonville, Oregon 97070

FDA Recall
Terminated ·PML, Inc. dba Pml Microbiologicals Inc.·Product code JTR·October 15, 2007

PML -- Vitek NH ID Card (NHI) Set - Quality Control kit for culture media. Each kit includes a 5 pack of LyfoCults Haemophilus parainfluenzae - Lot # 185-1 Exp 13AUG2008. PML Micrcobiologicals, 27120 SW 95th Avenue, Wilsonville, Oregon 97070

FDA Recall
Terminated ·PML, Inc. dba Pml Microbiologicals Inc.·Product code JTR·October 15, 2007

PML -- LyfoCults Haemophilus parainfluenzae - micro organism. Product label includes LyfoCults Haemophilus parainfluenzae ATCC 7901 Lot No.: 233851-1 Exp 05-17-09. PML Micrcobiologicals, 27120 SW 95th Avenue, Wilsonville, Oregon 97070

FDA Recall
Terminated ·PML, Inc. dba Pml Microbiologicals Inc.·Product code JTR·October 15, 2007

Brain Heart Infusion Agar (BHIA) + Vancomycin 6 MCG/ML Microbiological media plates

FDA Recall
Terminated ·Pml Microbiologicals Inc.·Product code JSO·August 17, 2007

Brain Heart Infusion Agar labeled BHIA + Vancomycin 6 MCG/ML For Screening for Vancomycin Resistant Enterococci PML microbiologicals Wilsonville, Oregon 97070 USA Catalog #P1174

FDA Recall
Terminated ·Pml Microbiologicals Inc.·Product code JSO·April 23, 2007

Software 1898072 IPC upgrade v 2.7.3.0, IPC System: a) CONSOLE 1898001 IPC, Product Number 1898001; b) CONSOLE IPC REFURB, Product Number EC300RF; c) MASTER CONSOLE EC300 LEGEND EHS, Product Number EC300

FDA Recall
Terminated ·Medtronic Xomed, Inc.·Product code ERL·December 15, 2021

Foot Control, SC2100 Product Usage: Electric system

FDA Recall
Terminated ·The Anspach Effort, Inc.·Product code ERL·October 6, 2016

Anspach Xmax Pneumatic Motor System; ENT Surgical Drill, including handpiece and Accessories Attached. All Models; Black Motors; Anspach Effort, Inc., Palm Beach FL 33410.

FDA Recall
Terminated ·The Anspach Effort, Inc.·Product code ERL·December 18, 2006

***REF XMAX***XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort, Inc. Intended for cutting and shaping bone.

FDA Recall
Terminated ·The Anspach Effort, Inc.·Product code ERL·April 25, 2013

ANSPACH, Rx only, Otologic Curved Micro (OCCM) Diamond Ball Burr, 1.5 MM, Part # OCM7-15SD Product Usage: The Otologic Curved Micro (OCCM) Attachment and burrs are intended for cutting and shaping bone primarily in otology procedures such as cochleostomies.

FDA Recall
Terminated ·The Anspach Effort, Inc.·Product code ERL·March 28, 2016

Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal, drilling and sawing of soft and hard tissue and bone in surgical procedures.

FDA Recall
Terminated ·Medtronic Xomed, Inc.·Product code ERL·June 12, 2020