239 results · 37ms · Sources: EU EUDAMED, US FDA

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BD Viper LT software, version 3.00H

FDA Recall
Terminated ·Bd Diagnostic·Product code OOI·December 14, 2015

BD Diagnostics, BD GeneOhm MRSA Assay, REF: 441242 (200 Reaction Kit) and 441244 (48 Reaction Kit). For the rapid detection of methicillin resistant MRSA DNA in nasal specimen.

FDA Recall
Terminated ·BD Diagnostics (GeneOhm Sciences, Inc)·Product code NQX·November 11, 2008

BD Vacutainer Push Button Blood collection Sets with Pre-Attached Holder; Catalog Number: 368656; 23 g X12 " PBBCS w/PAH (Preattached), BD Diagnostics, Franklin Lakes, NJ

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·November 20, 2007

BD Sensi-Disc Ticarcillin TIC-75, in vitro diagnostic, catalog # 231619, package of 10 cartridges, labeled in part ***BD Diagnostic Systems, 7 Loveton Circle, Sparks, MD 21152***

FDA Recall
Terminated ·Becton Dickinson & Co.·Product code JTN·February 19, 2007

BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX Enteric Bacterial Panel performed on the BD MAX System is an automated in vitro diagnostic test for the direct qualitative detection and differentiation of enteric bacterial pathogens.

FDA Recall
Terminated ·Becton Dickinson & Co.·Product code PIC·January 14, 2019

BD BACTEC FX 40 instrument, catalog number 442296, manufactured by BD Diagnostic Systems, 7 Loveton Circle, Sparks, MD 21152. The instrument is designed for the rapid detection of bacteria and fungi in clinical specimens. Samples are drawn from patients and injected directly into BACTEC culture vials, which are placed into the instrument for incubation and testing.

FDA Recall
Terminated ·Becton Dickinson & Co. BD Diagnostic Systems·Product code MDB·December 9, 2013

BD BACTEC FX- Top Unit instrument, catalog number 441385, and Bottom Unit instrument, catalog 441386, available as a single or a stack configuration; Manufactured by BD Diagnostic Systems, 7 Loveton Circle, Sparks, MD 21152. The BD BACTEC FX instrument is designed for the rapid detection of bacteria and fungi in clinical specimens. Samples are drawn from patients and injected directly into BACTEC culture vials, which are placed into the instrument for incubation and testing.

FDA Recall
Terminated ·Becton Dickinson & Co. BD Diagnostic Systems·Product code MDB·December 9, 2013

BD Focal Point"100V, Catalog number: 490650 The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"120V / 11 FOV (Refurbished), Catalog number: 490653. The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"230V / 15 FOV under 5%, Catalog number: 490137. The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"100V (Refurbished), Catalog number: 490651 The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"230V / 15 FOV (Refurbished), Catalog number: 490138. The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"230V / 11 FOV (Refurbished), Catalog number: 490649. The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"100V / 15 FOV under 5%, Catalog number: (Refurbished) 490365 The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"230V LC (Refurbished), Catalog number: 490681. The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"120V LC (Refurbished), Catalog number: 490683. The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"100V / 15 FOV under 5%, Catalog number: 490364 The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"120V / 15 FOV (Refurbished), Catalog number: 490398. The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"120v / 15 FOV under 5%, Catalog number: 490397. The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011

BD Focal Point"120V / 11 FOV under 5%, Catalog number: 490652 The BD Focal Point" Slide Profiler (formerly the AutoPap System) is an automated cervical cytology screening device intended for use in initial screening of cervical cytology slide.

FDA Recall
Terminated ·Tripath Imaging, Inc.·Product code MKQ·October 6, 2011