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VITROS Anti-HBs Calibrators & VITROS Anti-HBs Reagent Packs

FDA Recall
Terminated ·Ortho-Clinical Diagnostics·Product code LOM·October 25, 2013

Conformis iTotal Hip Replacement System: HBS-033-00xx-010101, (HIP-PATIENT SPECIFIC STEM LEFT)

FDA Enforcement
Class II ·Terminated·Conformis, Inc.·June 19, 2019

Conformis iTotal Hip Replacement System: HBS-033-00xx-020101, (HIP-PATIENT SPECIFIC STEM RIGHT)

FDA Enforcement
Class II ·Terminated·Conformis, Inc.·June 19, 2019

The spare component Anti-HBs Cutoff Calibrator, 10 mLU/mL, Catalog number 26154. The spare component is sold separately from the MONOLISA Anti-HBs EIA Kit contains an expiration date of 2016-04-30 in error.

FDA Recall
Terminated ·Bio-Rad Laboratories, Inc.·Product code JJX·May 13, 2015

VITROS Anti-HBs Calibrators & VITROS Anti-HBs Reagent Packs

FDA Enforcement
Class II ·Terminated·Ortho-Clinical Diagnostics·January 1, 2014

VITROS¿ Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B surface antigen (anti-HBs)) Reagent Packs For the quantitative in vitro determination of total antibody to hepatitis B surface antigen (anti-HBs) in human serum.

FDA Enforcement
Class III ·Terminated·Ortho-Clinical Diagnostics·May 1, 2013

VITROS Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B surface antigen (anti-HBs)) Reagent Packs For the quantitative in vitro determination of total antibody to hepatitis B surface antigen (anti-HBs) in human serum.

FDA Recall
Terminated ·Ortho-Clinical Diagnostics·Product code LOM·November 1, 2012

Bio-Rad's Monolisa (TM) Anti-HBs EIA test kit, Labeled as, "MONOLISA TM Anti-HBs EIA 25220; MONOLISA TM Anti-HBs Calibrator Kit 25219... Bio-Rad Laboratories Redmond, WA 98052" For the qualitative detection of antibody to Hepatitis B Surface Antigen (anti-HBs) in Human Serum and EDTA or citrated plasma.

FDA Recall
Terminated ·Bio-Rad Laboratories·Product code LOM·August 11, 2008

The spare component Anti-HBs Cutoff Calibrator, 10 mLU/mL, Catalog number 26154. The spare component is sold separately from the MONOLISA Anti-HBs EIA Kit contains an expiration date of 2016-04-30 in error.

FDA Enforcement
Class III ·Terminated·Bio-Rad Laboratories, Inc.·July 1, 2015

The Bio-Rad MONOLISA Anti-HBs EIA is for In Vitro Diagnostic Use and it has the catalog number 25220. It is a qualitative and quantitative enzyme immunoassay for the detection of antibody for hepatitis B surface antigen in human serum and EDTA or citrated plasma. The Bio-Rad MONOLISA Anti-HBs EIA is a qualitative and quantitative enzyme immunoassay for the detection of antibody for hepatitis B surface antigen in human serum and EDTA or citrated plasma. The assay results may be used as an aid in the determination of susceptibility to hepatitis B virus (HBV) infection in individuals prior to or following HBV vaccination or where vaccination status is unknown. Assay results may be used with other HBV serological markers for the laboratory diagnosis of HBV disease associated with HBV infection.

FDA Recall
Terminated ·Bio-Rad Laboratories·Product code LOM·July 27, 2012

K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine.

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·August 21, 2019

K-Wire HBS Sterile Lot, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·August 21, 2019

The Bio-Rad MONOLISA Anti-HBs EIA is for In Vitro Diagnostic Use and it has the catalog number 25220. It is a qualitative and quantitative enzyme immunoassay for the detection of antibody for hepatitis B surface antigen in human serum and EDTA or citrated plasma. The Bio-Rad MONOLISA Anti-HBs EIA is a qualitative and quantitative enzyme immunoassay for the detection of antibody for hepatitis B surface antigen in human serum and EDTA or citrated plasma. The assay results may be used as an aid in the determination of susceptibility to hepatitis B virus (HBV) infection in individuals prior to or following HBV vaccination or where vaccination status is unknown. Assay results may be used with other HBV serological markers for the laboratory diagnosis of HBV disease associated with HBV infection.

FDA Enforcement
Class II ·Terminated·Bio-Rad Laboratories·September 26, 2012

K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine.

FDA Recall
Terminated ·BioPro, Inc.·Product code NBH·June 25, 2019

K-Wire HBS Sterile Lot, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

FDA Recall
Terminated ·BioPro, Inc.·Product code NBH·June 25, 2019

FSE Image Upgrade Kit, Catalog # 92019C This kit is used to install and/or upgrade software used with the EVOLIS Microplate System.

FDA Recall
Terminated ·Bio-Rad Laboratories·Product code LOM·August 20, 2013

iTotal Hip Replacement System, Model HBS-033-0015-020101, Size 15 Hip-Patient Specific Stem Right

FDA Enforcement
Class II ·Terminated·Conformis, Inc.·October 16, 2019

iTotal Hip Replacement System, Model HBS-033-0013-020101, Size 13 Hip-Patient Specific Stem Right

FDA Enforcement
Class II ·Terminated·Conformis, Inc.·October 16, 2019

Go-EZ Screw 6.5x90, Item Number 19666 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·August 21, 2019

Go-EZ Screw 6.5x110, Item Number 19670 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·August 21, 2019