BEUDAMED
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    bioMrieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent cards designed for the ID and antimicrobial susceptibility testing of bacteria and yeast.

    FDA Recall
    Terminated ·Biomerieux Inc·Product code JST·January 23, 2018

    Endoscopic Curved Needle, Surgical Needle Guide, Supplied sterilized by ethylene oxide gas in peel-open packages. Used for internal suturing under direct vision during intraabdominal endoscopic procedures. The needle driver design affords precise placement and control of standard curved suture needles, similar to open abdominal suturing.

    FDA Enforcement
    Class II ·Terminated·Cook Inc.·June 14, 2017

    ST-AIA PACK HGH; Part Number: 025266 Assay, Metabolic

    FDA Enforcement
    Class II ·Terminated·Tosoh Bioscience Inc·June 13, 2018

    The VITEK 2 Neisseria-Haemophilus identification card (NH) is intended for use with the VITEK 2 Systems for the automated identification of most clinically significant fastidious organisms. The VITEK 2 NH identification card is a single-use disposable. A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.

    FDA Enforcement
    Class II ·Terminated·BioMerieux SA·June 20, 2018

    AF 550 x 5ML/H FH DL 30hole SAT C,4"IN, Product code MC0050XLYK2 CP, Arrow AutoFuser Disposable Pain Control Pump

    FDA Enforcement
    Class II ·Terminated·Arrow International Inc·March 6, 2019

    bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent cards designed for the ID and antimicrobial susceptibility testing of bacteria and yeast.

    FDA Enforcement
    Class II ·Terminated·Biomerieux Inc·August 29, 2018

    Vapotherm Precision Flow,Disposable Patient Circuit PF-E-DPC-Low. PF-DPC-Low packaged with compatible cannulas for evaluation of the Precision Flow system

    FDA Enforcement
    Class II ·Terminated·Vapotherm, Inc.·October 1, 2014

    Vapotherm Precision Flow,Disposable Patient Circuit PF-NODPC-Low. For use with the Precision Flow system and Ikaria INOmax DSIR ¿ System. This DPC allows clinicians to administer nitric oxide non-invasively via high flow nasal cannula. In the Precision Flow High Flow Therapy application, a special disposable patient circuit re-routes the gas to the INOmax injector module then back into the Precision Flow system

    FDA Enforcement
    Class II ·Terminated·Vapotherm, Inc.·October 1, 2014

    Vapotherm Precision Flow,Disposable Patient Circuit PF-E-DPC-High. For use with the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in the hospital, sub-acute institutions, and home settings. It adds heat and moisture to blended medical air/oxygen mixture and assures the integrity of the precise air/oxygen mixture via an integral oxygen analyzer. The flow rates may be from 1 to 40 liters per minute via nasal cannula.

    FDA Enforcement
    Class II ·Terminated·Vapotherm, Inc.·October 1, 2014

    Vapotherm Precision Flow,Disposable Patient Circuit PFHDPC-Low. For use with the Heliox Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in the hospital, sub-acute institutions, and home settings. It adds heat and moisture to blended medical air/oxygen mixture and assures the integrity of the precise air/oxygen mixture via an integral oxygen analyzer. The flow rates may be from 1 to 40 liters per minute via nasal cannula.

    FDA Enforcement
    Class II ·Terminated·Vapotherm, Inc.·October 1, 2014

    Vapotherm Precision Flow,Disposable Patient Circuit PFH-DPC-High. For use with the Heliox Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in the hospital, sub-acute institutions, and home settings. It adds heat and moisture to blended medical air/oxygen mixture and assures the integrity of the precise air/oxygen mixture via an integral oxygen analyzer. The flow rates may be from 1 to 40 liters per minute via nasal cannula.

    FDA Enforcement
    Class II ·Terminated·Vapotherm, Inc.·October 1, 2014

    Vapotherm Precision Flow, Disposable Patient Circuit PF-DPC-High. For use with the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in the hospital, sub-acute institutions, and home settings. It adds heat and moisture to blended medical air/oxygen mixture and assures the integrity of the precise air/oxygen mixture via an integral oxygen analyzer. The flow rates may be from 1 to 40 liters per minute via nasal cannula.

    FDA Enforcement
    Class II ·Terminated·Vapotherm, Inc.·October 1, 2014

    Vapotherm Precision Flow,Disposable Patient Circuit PF-DPC-Low. For use with the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in the hospital, sub-acute institutions, and home settings. It adds heat and moisture to blended medical air/oxygen mixture and assures the integrity of the precise air/oxygen mixture via an integral oxygen analyzer. The flow rates may be from 1 to 40 liters per minute via nasal cannula.

    FDA Enforcement
    Class II ·Terminated·Vapotherm, Inc.·October 1, 2014

    Vapotherm Precision Flow,Disposable Patient Circuit PFNODPC-High. For use with the Precision Flow system and Ikaria INOmax DSIR ¿ System. This DPC allows clinicians to administer nitric oxide non-invasively via high flow nasal cannula. In the Precision Flow High Flow Therapy application, a special disposable patient circuit re-routes the gas to the INOmax injector module then back into the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in the hospital, sub-acute institutions, and home settings. It adds heat and moisture to blended medical air/oxygen mixture and assures the integrity of the precise air/oxygen mixture via an integral oxygen analyzer. The flow rates may be from 1 to 40 liters per minute via nasal cannula.

    FDA Enforcement
    Class II ·Terminated·Vapotherm, Inc.·October 1, 2014

    StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for cranial procedures using optical localization StealthStation Cranial version 3.0, 3.1 CE 0344 Rx Only 2018-02 9735489 Revision 3 Medtronic Navigation, Inc. Biopsy Needle Kit (9733068) Note: This device is an accessory to your StealthStation System. . . The Biopsy Needle is a presterilized , single-use, side-cutting needle for cranial tissue biopsies. CE 0344 Rx Only 2017-05 9733068-01 Medtronic Navigation, Inc.

    FDA Enforcement
    Class I ·Terminated·Medtronic Navigation, Inc.·January 9, 2019

    Lactate Gen.2, Catalog Nos. 03183700190, 05171881190, 11822837190, ***added as of 5/10/19*** 03183700190 Product Usage: An In vitro diagnostic reagent system intended for use on cobas Integra for the quantitative determination of the lactate concentration in plasma and cerebrospinal fluid.

    FDA Recall
    Terminated ·Roche Diagnostics Corporation·Product code KHP·December 17, 2018

    The VITEK 2 Neisseria-Haemophilus identification card (NH) is intended for use with the VITEK 2 Systems for the automated identification of most clinically significant fastidious organisms. The VITEK 2 NH identification card is a single-use disposable. A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.

    FDA Recall
    Terminated ·BioMerieux SA Chemin De L'Orme Marcy L'Etoile France·Product code JST·March 23, 2018

    Tina-quant IgM Gen.2, Catalog Nos. 03507190190, 05220726190, 03507041190, 03507149190 Product Usage: Immunoturbidimetric assay for the quantitative in vitro determination of IgM in human serum and plasma on automated clinical chemistry analyzers analyzers.

    FDA Recall
    Terminated ·Roche Diagnostics Corporation·Product code DAQ·December 17, 2018

    Bilirubin Total Gen.3, Cat. Nos. 05795397190, 05795419190, 05795320160, 05795338160, 05795346160 ***added as of 5/10/19***05795397190, 05795648190 Product Usage: In vitro test for the quantitative determination of total bilirubin in serum and plasma of adults and neonates on Roche/Hitachi cobas c systems.

    FDA Recall
    Terminated ·Roche Diagnostics Corporation·Product code CIG·December 17, 2018

    Boston Scientific, IMAGER II Angiographic Catheter, Sterilized with ethylene oxide gas. Made in Ireland, Manufactured for Boston Scientific Corporation, One Boston Scientific Place, Natick, MA 01760-1537. The following product is being recalled: "Material Number/(OUTER CARTON LABEL OF 5pk)"/"Material Number (INNER-POUCH LABEL FOR EACH SINGLE CATHETER)" / Material Description / Catalog Number. M001314001 M001314000 IMAGER II/5/ST/65/038 BX5 31-400 M001314011 M001314010 IMAGER II/5/ST/100/038 BX5 31-401 M001314021 M001314020 IMAGER II/5/ST/65/035 BX 5 31-402 M001314031 M001314030 IMAGER II/5/ST/100/035 BX 5 31-403 M001314041 M001314040 IMAGER II/5/BARNH/100/038 BX5 31-404 M001314051 M001314050 IMAGER II/5/BERN/100/038 BX5 31-405 M001314061 M001314060 IMAGER II/5/BERN/100/035 BX 5 31-406 M001314071 M001314070 IMAGER II/5/BERN/40/035 BX 5 31-407 M001314081 M001314080 IMAGER II/5/BERN/40/038 BX5 31-408 M001314091 M001314090 IMAGER II/5/BERN/65/035 BX 5 31-409 M001314101 M001314100 IMAGER II/5/BERN/65/038 BX5 31-410 M001314111 M001314110 IMAGER II/5/WEIN/100/038 BX5 31-411 M001314121 M001314120 IMAGER II/5/WEIN/100/035 BX 5 31-412 M001314131 M001314130 IMAGER II/5/H1/65/038 BX5 31-413 M001314141 M001314140 IMAGER II/5/H1/100/038 BX5 31-414 M001314151 M001314150 IMAGER II/5/H1/100/035 BX 5 31-415 M001314161 M001314160 IMAGER II/5/H3/100/038 BX5 31-416 M001314171 M001314170 IMAGER II/5/H3/100/035 BX 5 31-417 M001314181 M001314180 IMAGER II/5/H1H/100/038 BX5 31-418 M001314191 M001314190 IMAGER II/5/H1H/100/035 BX 5 31-419 M001314201 M001314200 IMAGER II/5/H3H/100/035 BX 5 31-420 M001314211 M001314210 IMAGER II/5/JB1/65/038 BX5 31-421 M001314221 M001314220 IMAGER II/5/JB1/100/038 BX5 31-422 M001314231 M001314230 IMAGER II/5/JB1/100/035 BX 5 31-423 M001314241 M001314240 IMAGER II/5/JB2/100/038 BX5 31-424 M001314251 M001314250 IMAGER II/5/JB2/100/035 BX 5 31-425 M001314261 M001314260 IMAGER II/5/JB3/100/038 BX5 31-426 M001314271 M001314270 IMAGER II/5/JB3/100/035 BX 5 31-427 M001314281 M001314280 IMAGER II/5/MAN/100/038 BX5 31-428 M001314291 M001314290 IMAGER II/5/MAN/100/035 BX 5 31-429 M001314301 M001314300 IMAGER II/5/SIM1/65/038 BX5 31-430 M001314311 M001314310 IMAGER II/5/SIM1/65/035 BX 5 31-431 M001314321 M001314320 IMAGER II/5/SIM1/100/038 BX5 31-432 M001314331 M001314330 IMAGER II/5/SIM1/100/035 BX 5 31-433 M001314341 M001314340 IMAGER II/5/SIM2/100/038 BX5 31-434 M001314351 M001314350 IMAGER II/5/SIM2/100/035 BX 5 31-435 M001314361 M001314360 IMAGER II/5/SIM3/100/038 BX5 31-436 M001314371 M001314370 IMAGER II/5/SIM3/100/035 BX 5 31-437 M001314381 M001314380 IMAGER II/5/SIM4/100/038 BX5 31-438 M001314391 M001314390 IMAGER II/5/HN1/100/038 BX5 31-439 M001314401 M001314400 IMAGER II/5/HN1/100/035 BX 5 31-440 M001314411 M001314410 IMAGER II/5/HN2/100/038 BX5 31-441 M001314421 M001314420 IMAGER II/5/HN2/100/035 BX 5 31-442 M001314431 M001314430 IMAGER II/5/HN3/100/038 BX5 31-443 M001314441 M001314440 IMAGER II/5/HN3/100/035 BX 5 31-444 M001314451 M001314450 IMAGER II/5/HN4/100/038 BX5 31-445 M001314461 M001314460 IMAGER II/5/HN4/100/035 BX 5 31-446 M001314471 M001314470 IMAGER II/5/HN5/100/038 BX5 31-447 M001314481 M001314480 IMAGER II/5/HN5/100/035 BX 5 31-448 M001314491 M001314490 IMAGER II/5/CK/100/035 BX 5 31-449 M001314501 M001314500 IMAGER II/5/GEN/100/035 BX 5 31-450 M001314511 M001314510 IMAGER II/5/GEN+2 SIDEHOLES/100/035 BX 5 31-451 M001314521 M001314520 IMAGER II/5/CHGB/65/038 BX5 31-452 M001314531 M001314530 IMAGER II/5/CHGB/65/035 BX 5 31-453 M001314541 M001314540 IMAGER II/5/CHGC/65/038 BX5 31-454 M001314551 M001314550 IMAGER II/5/CHGC/65/035 BX 5 31-455 M001314561 M001314560 IMAGER II/5/CHG2.5/65/038 BX5 31-456 M001314571 M001314570 IMAGER II/5/CHG2.5/65/035 BX 5 31-457 M001314581 M001314580 IMAGER II/5/CONTRA 2/65/038 BX5 31-458 M001314591 M001314590 IMAGER II/5/CONTRA 2/65/035 BX 5 31-459 M001314611 M001314610 IMAGER II/5/DUCK/65/035 BX 5 31-4

    FDA Recall
    Terminated ·Boston Scientific Corporation·Product code DQO·March 15, 2012