21 results
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21ms
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Sources: EU EUDAMED, US FDA
HOTLlNE Disposable Administration Sets, Product Code L-370 Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE Routine Flow Blood and Fluid Warmers (HL-90 and HL-290), for the warming and delivery of blood and I.V. solutions, at normothermic flow rates of 50 - 5,000 ml/hr.
FDA Recall
Terminated
·Smiths Medical ASD, Inc.·Product code LGZ·November 21, 2011
HOTLlNE Disposable Administration Sets, Product Codes L-70NI Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE Routine Flow Blood and Fluid Warmers (HL-90 and HL-290), for the warming and delivery of blood and I.V. solutions, at normothermic flow rates of 50 - 5,000 ml/hr.
FDA Recall
Terminated
·Smiths Medical ASD, Inc.·Product code LGZ·November 21, 2011
HOTLlNE Disposable Administration Sets, Product Code L-80 Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE Routine Flow Blood and Fluid Warmers (HL-90 and HL-290), for the warming and delivery of blood and I.V. solutions, at normothermic flow rates of 50 - 5,000 ml/hr.
FDA Recall
Terminated
·Smiths Medical ASD, Inc.·Product code LGZ·November 21, 2011
Level 1 Normothermic I.V. Fluid Administration Sets, Product Code D-60HL , Product Usage: Single patient use sets designed for use by trained medical professionals, in conjunction with Level 1 Fast Flow Fluid Warmers (H1000, H-1025, H-1028, and H-1200), for the warming and delivery of blood and I.V. solutions, at flow rates of 75ml/min - 530 ml/min.
FDA Recall
Terminated
·Smiths Medical ASD, Inc.·Product code LGZ·November 21, 2011
Level 1 Normothermic I.V. Fluid Administration Sets, Product Code DI-60HL , Product Usage: Single patient use sets designed for use by trained medical professionals, in conjunction with Level 1 Fast Flow Fluid Warmers (H1000, H-1025, H-1028, and H-1200), for the warming and delivery of blood and I.V. solutions, at flow rates of 75ml/min - 530 ml/min.
FDA Recall
Terminated
·Smiths Medical ASD, Inc.·Product code LGZ·November 21, 2011
HOTLlNE Disposable Administration Sets, Product Code L-270 Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE Routine Flow Blood and Fluid Warmers (HL-90 and HL-290), for the warming and delivery of blood and I.V. solutions, at normothermic flow rates of 50 - 5,000 ml/hr.
FDA Recall
Terminated
·Smiths Medical ASD, Inc.·Product code LGZ·November 21, 2011
HOTLlNE Disposable Administration Sets, Product Codes L-70 Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE Routine Flow Blood and Fluid Warmers (HL-90 and HL-290), for the warming and delivery of blood and I.V. solutions, at normothermic flow rates of 50 - 5,000 ml/hr.
FDA Recall
Terminated
·Smiths Medical ASD, Inc.·Product code LGZ·November 21, 2011
VITROS 4600 Chemistry System, Software Version 3.2 & Below. Automates pre-analytical and post-analytical sample and data management for in vitro diagnostic use.
FDA Recall
Terminated
·Ortho-Clinical Diagnostics·Product code JJE·April 6, 2015
VITROS 5600 Chemistry System, Software Version 3.2 & Below. Automates pre-analytical and post-analytical sample and data management for in vitro diagnostic use.
FDA Recall
Terminated
·Ortho-Clinical Diagnostics·Product code JJE·April 6, 2015
3D-I/III Ceiling Stand. Diagnostic x-ray tube mount
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYB·April 28, 2006
ORTHOLOC 3DI PLT SYS STERILE, LOCKING SCREW, 3.5 x 38mm Sterile, Part Number 58S03538
FDA Recall
Terminated
·Wright Medical Technology, Inc.·Product code HWC·November 8, 2016
bioMerieux Kit, Instrument & Update, B.40, 3D I ZIP-ML01, Industry instrument software update, English, Spanish, Italian, catalog number 413483 Software update for an instrument which is most commonly used to isolate and recover specimens drawn from adult and older pediatric patients that are acutely ill with signs and symptoms suggestive of blood stream infection, which can be due to a variety of sources including lung, abdomen, urinary tract, endovascular, and skin.
FDA Recall
Terminated
·Biomerieux Inc·Product code MDB·October 16, 2012
bioMerieux Kit, Instrument & Update, B.40, 3D I USB-ML02, Industry instrument software update, German, French, catalog number 413482 Software update for an instrument which is most commonly used to isolate and recover specimens drawn from adult and older pediatric patients that are acutely ill with signs and symptoms suggestive of blood stream infection, which can be due to a variety of sources including lung, abdomen, urinary tract, endovascular, and skin.
FDA Recall
Terminated
·Biomerieux Inc·Product code MDB·October 16, 2012
bioMerieux Kit, Instrument & Update, B.40, 3D I ZIP-ML02, Industry instrument software update, English, Spanish, Italian, catalog number 413484 Software update for an instrument which is most commonly used to isolate and recover specimens drawn from adult and older pediatric patients that are acutely ill with signs and symptoms suggestive of blood stream infection, which can be due to a variety of sources including lung, abdomen, urinary tract, endovascular, and skin.
FDA Recall
Terminated
·Biomerieux Inc·Product code MDB·October 16, 2012
bioMerieux Kit, Instrument & Update, B.40, 3D I USB-ML01, Industry instrument software update, English, Spanish, Italian, catalog number 413481 Software update for an instrument which is most commonly used to isolate and recover specimens drawn from adult and older pediatric patients that are acutely ill with signs and symptoms suggestive of blood stream infection, which can be due to a variety of sources including lung, abdomen, urinary tract, endovascular, and skin.
FDA Recall
Terminated
·Biomerieux Inc·Product code MDB·October 16, 2012
Tina-quant Complement C4 ver.2, Catalog 05991994190
FDA Recall
Terminated
·Roche Diagnostics Operations, Inc.·Product code DBI·August 27, 2020
C4 is an in vitro diagnostic assay for the quantitative determination of C4 in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light scattering, measured by reading turbidity at 604 nm, which correlates with the concentration of C4 in the sample.
FDA Recall
Terminated
·Abbott Laboratories, Inc·Product code DBI·May 16, 2018
Access Immunoassay Systems Thyroglobulin Antibody Reagent Kit, Part Number 33890
FDA Recall
Terminated
·Beckman Coulter Inc·Product code DDC·October 26, 2006
One heart and pericardium from donor 12144.
FDA Recall
Terminated
·DCI Donor Services Tissue Services Division·Product code MIE·August 20, 2002
Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals to illuminate the oral cavity while performing examinations and dental procedures.
FDA Recall
Terminated
·Pelton & Crane Marus DCI Equipment KaVo·Product code EAZ·March 8, 2016