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0320,APS1,08,N,RD,RM

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828151504·0320,APS1,08,N,RD,RM

1801,APS0,08,N,RD,RM

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828150835·1801,APS0,08,N,RD,RM

1802,APS1,08,N,RD,RM,RYL

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828150965·1802,APS1,08,N,RD,RM,RYL

ALINITY C PROCESSING MODULE

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·June 9, 2024

0412,APS1,08,N,RD ON/OFF,RM ON/OFF

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828152358·0412,APS1,08,N,RD ON/OFF,RM ON/OFF

SYSTEM, APPENDAGE CLOSURE, LEFT ATRIAL

FDA Adverse Event
Death ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·September 22, 2025

SYSTEM, APPENDAGE CLOSURE, LEFT ATRIAL

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·September 22, 2025

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·November 18, 2013

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·August 14, 2009

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·August 14, 2009

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·September 25, 2009

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·August 14, 2009

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·August 14, 2009

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·August 14, 2009

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·August 14, 2009

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·August 14, 2009

ORTHO PROVUE ANALYZER

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 30, 2006

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·June 26, 2008

BD SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·January 15, 2026

MATRX

FDA Adverse Event
Malfunction ·MIDMARK CORP.·Product code NRD·May 18, 2011