75 results
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15ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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Cardio Medical Products, Inc. Defibrillation/Cardioversion/Monophasic or Biphasic Pacing/ECG Electrode Rx Only Single Patient Use Only Manufactured for Cardio Medical Products 385 Franklin Avenue, Suite L Rockaway, New Jersey 07866 www.cardiomedicalproducts.com (800) 227-3633 (973) 586-9624 FAX Defibrillator
FDA Recall
Terminated
·Cardio Medical Products·Product code LDD·April 26, 2013
Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.
FDA Recall
Terminated
·Covidien LLC·Product code DRO·April 8, 2013
Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles
FDA Recall
Terminated
·Covidien LLC·Product code LRO·September 29, 2016
Covidien Devon Light Glove packaged in sterile surgical kits Reference: 31140208 Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles
FDA Recall
Terminated
·Covidien LLC·Product code LRO·September 29, 2016
Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode Product ID: 22550P. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.
FDA Recall
Terminated
·Covidien LLC·Product code DRO·April 8, 2013
MEDPOR PLUS SST EZ 22mm Sphere Implant, Howmedica Osteonics Corp, 15 Dart Road, Newnan, GA 30265. MEDPOR PLUS Orbital Implants are intended to restore the volume of an enucleated or eviscerated eye globe.
FDA Recall
Terminated
·Howmedica Osteonics Corp dba Stryker Craniomaxillofacial·Product code HPZ·March 20, 2012
QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes (Sterile) Accessories to TLS Surgical Drainage System
FDA Recall
Terminated
·Stryker Leibinger GmbH & Co. KG Botzinger Strasse 41 Freiburg Germany·Product code GCY·January 3, 2017
Professional Hospital Supply, Inc Custom Packaging containing the Devon Light Glove Item Number Description 380789003 SURE SET SINGLE BASIN PACK 400383006 MAJOR BASIN PACK 400383007 MAJOR BASIN PACK 618275004 BASIN PACK Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles
FDA Recall
Terminated
·Covidien LLC·Product code LRO·September 29, 2016
9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design M Malar Sizer Set (Silicone, Non-Sterile) 9952 Extended Contoured, Malar Sizer Set (Silicone, Non-Sterile) 85000 Petite Nasal Dorsum Sizer Set (Silicone, Non-Sterile) Accessories to Medpor Implants
FDA Recall
Terminated
·Stryker Leibinger GmbH & Co. KG Botzinger Strasse 41 Freiburg Germany·Product code GCY·January 3, 2017
MONOJECT Blood Collection Tubes containing heparin 10x64 Sodium Heparin Item code 8881320256
FDA Recall
Terminated
·Product code JKA·November 15, 2010
MONOJECT Blood Collection Tubes containing heparin 13x100 sodium heparin trace element Item Code 8881307014
FDA Recall
Terminated
·Product code JKA·November 15, 2010
MONOJECT Blood Collection Tubes containing heparin 10x50 Sodium Heparin Item code 8881320157
FDA Recall
Terminated
·Product code JKA·November 15, 2010
MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. MEDPOR Surgical Implants and MEDPOR BARRIER Implants are intended for the augmentation or restoration of bony contour in the craniofacial skeleton.
FDA Recall
Terminated
·Stryker Craniomaxillofacial Division·Product code FWP·December 17, 2014
MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. MEDPOR Surgical Implants and MEDPOR BARRIER Implants are intended for the augmentation or restoration of bony contour in the craniofacial skeleton.
FDA Recall
Terminated
·Stryker Craniomaxillofacial Division·Product code FWP·December 17, 2014
MediChoice Multifunction Electrode Part Number: MC171 OH
FDA Recall
Terminated
·Covidien LLC·Product code MKJ·September 18, 2014
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. MEDPOR Surgical Implants and MEDPOR BARRIER Implants are intended for the augmentation or restoration of bony contour in the craniofacial skeleton.
FDA Recall
Terminated
·Stryker Craniomaxillofacial Division·Product code FWP·December 17, 2014
MONOJECT Prefill Heparin Lock Flush Syringe 10 Unit Heparin, 3 ml in 12 ml syringe Item code 8881580123
FDA Recall
Terminated
·Product code NGT·November 15, 2010
MONOJECT Prefill Heparin Lock Flush Syringe 100 Unit Heparin, 3 ml in 12 ml syringe Item code 8881590123
FDA Recall
Terminated
·Product code NGT·November 15, 2010
MONOJECT Prefill Heparin Lock Flush Syringe 100 Unit Heparin, 10 ml in 12 ml syringe Item code 8881590121
FDA Recall
Terminated
·Product code NGT·November 15, 2010
MONOJECT Prefill Heparin Lock Flush Syringe 10 Unit Heparin, 5 ml in 12 ml syringe Item code 8881580125
FDA Recall
Terminated
·Product code NGT·November 15, 2010