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BD Vacutainer PST Blood Collection Tubes, Catalog Number 368035, 368036

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·June 12, 2019

BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog Number: 365987

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·May 13, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes, Catalog Number 367963

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·June 12, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 65 Units Blood Collection Tubes, Catalog Number 367961

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·June 12, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes, Catalog Number 367962

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·June 12, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 368056

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·June 12, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection Tubes, Catalog Number 367964

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·June 12, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 367960

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·June 12, 2019

BD Vacutainer PST Tubes (GOLD TOP PST TUBE 3ml) Part Number: BD 367960 FMC part Number: 87-4544-4 Single use tube used to collect, separate, transport or process blood specimens for laboratory determinations for in vitro diagnostic use. The concentrate is formulated to be used with a three steam hemodialysis machine which is calibrated for acid and bicarbonate concentrates.

FDA Recall
Terminated ·Fresenius Medical Care Holdings, Inc.·Product code JKA·June 23, 2014

CoaguChek XS PST Meters- IVD (Patient Self-Testing) measures blood-clotting time for people who are taking anticoagulation medications such as Coumadin or warfarin. Catalog 04837738001

FDA Recall
Terminated ·Roche Diagnostics Operations, Inc.·Product code GJS·December 2, 2020

RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.

FDA Recall
Terminated ·Mako Surgical Corporation·Product code OLO·February 23, 2016

RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.

FDA Recall
Terminated ·Mako Surgical Corporation·Product code OLO·October 7, 2014

RESTORIS PST Acetabular Straight Shell Impactors An impactor is a reusable instrument designed for use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.

FDA Recall
Terminated ·Mako Surgical Corporation·Product code OLO·October 7, 2014

RESTORIS PST Acetabular Offset Shell Impactors An impactor is a reusable instrument designed for use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.

FDA Recall
Terminated ·Mako Surgical Corporation·Product code OLO·October 7, 2014

Roche CoaguChek XS System, CoaguChek XS PST Kit, Roche Diagnostics, Indianapolis, IN; Catalog/Model Number 04837738001. CoaguChek XS System and CoaguChek XS Plus System are point of care monitoring devices for people taking oral anticoagulation medication.

FDA Recall
Terminated ·Roche Diagnostics Operations, inc.·Product code GJS·July 22, 2009

CoaguChek XS System (PST) The CoaguChek XS PT test strips are part of the CoaguChek XS System. The CoaguChek XS System measures blood-clotting time for people who are taking anticoagulation medications such as Coumadin or warfarin.

FDA Recall
Terminated ·Roche Diagnostics Operations, Inc.·Product code GJS·May 16, 2013

BD Vacutainer PST Gel and Lithium Heparin (LH); 83 Units; Plus Blood Collection Tubes; Sterile; IVD; REF 367962; 4.5 mL, 13 X 100 mm; BD, Franklin Lakes, NJ USA; Made in USA. Used in hospitals, outpatient clinics and physicians' offices to collect blood from patients for specialized chemistry testing.

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·March 5, 2012

Natrelle 133 Series Tissue Expanders Product Usage: Natrelle 133 Series Tissue Expander is intended for temporary subcutaneous implantation and require periodic, incremental inflation with sterile saline for injection until the desired amount of tissue is developed.

FDA Recall
Terminated ·Allergan Inc·Product code LCJ·June 18, 2015

Natrelle Re-sterilizable Breast Implant Sizer, Size: 410 cc, Style No. MSZFX410. The product is packaged in a thermoformed tray (double sterile barrier) and enclosed in a labeled carton.

FDA Recall
Terminated ·Allergan Inc·Product code MRD·June 8, 2015

Natrelle CUI Series Tissue Expanders. Product Usage: Natrelle CUI Series Tissue Expander has been designed for temporary implantation to develop a skin flap. The device is used for reconstructive correction of a defect or to provide cover for a prosthetic implant. The CUI Tissue Expander consists of a silicone elastomer envelope and a remote injection port.

FDA Recall
Terminated ·Allergan Inc·Product code LCJ·June 18, 2015