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    ROHO HIGH PROFILE Single Compartment Cushion with Sensor Ready Technology and ROHO MID PROFILE Single Compartment Cushion with Sensor Ready Technology.

    FDA Recall
    Terminated ·Roho Inc.·Product code KIC·March 20, 2017

    Automated Impella Controller (AIC), Product No. 0042-0000-US, 0042-0010-US, 0042-0040-US. Used with Impella Ventricular Support Systems (cardiovascular)

    FDA Recall
    Terminated ·Abiomed, Inc.·Product code OZD·March 1, 2021

    Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code JXG·April 21, 2014

    Automated Impella Controller (AIC), product number 0042-040-US with software versions V8.4 and V8.4.1.

    FDA Recall
    Terminated ·Abiomed, Inc.·Product code OZD·October 10, 2023

    Automated Impella Controller (AIC), product number 0042-000-US with software versions V8.4 and V8.4.1.

    FDA Recall
    Terminated ·Abiomed, Inc.·Product code OZD·October 10, 2023

    Vein Irrigation Cannula with blunt tip. ASY BIC, STERILE 25/CS REF/ GTIN for Insert Label:BIC/ 00803622133091

    FDA Recall
    Terminated ·LivaNova USA Inc.·Product code DWF·April 24, 2020

    Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of the brain into the peritoneum.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code JXG·November 11, 2014

    The Dual Switch Valve is used for fluid drainage from the ventricles into the peritoneum, in cases of hydrocephalus.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code JXG·October 24, 2014

    Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS, non-sterile, non-absorbable polyamide Surgical Suture, additional label affixed on the box states the product is sterile, packaged in a cassette holding 12 sutures

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code GAR·June 13, 2014

    CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM REF: PL731SU- Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.

    FDA Recall
    Terminated ·Aesculap Implant Systems LLC·Product code GEI·August 7, 2019

    CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.

    FDA Recall
    Terminated ·Aesculap Implant Systems LLC·Product code GEI·August 7, 2019

    Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with the HiLAN and microspeed motor systems to hold burrs which cut and shape bone.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code GET·December 9, 2013

    Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (BIC) - VERSION 2, Article Code Number 3456102A. These conductivity sensors may be used as spare parts for the following dialysis machines: 710200L (UDI 04046963686345), 710200S (UDI 04046964285608), 710200U (UDI 04046964285615), 710200K (UDI 04046963686338), 710500L (UDI Not applicable) and 710500K (UDI Not applicable).

    FDA Recall
    Terminated ·B Braun Medical Inc·Product code KDI·January 28, 2022

    Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code JXG·December 23, 2013

    PRE2055: Prevena Customizable Dressing 5-Pack Product Usage: The Prevena Incision Management System is intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed environment and removing exudates via the application of negative pressure wound therapy.

    FDA Recall
    Terminated ·KCI USA, INC.·Product code OMP·January 30, 2014

    AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #M4268882 used with InfoVAC Model M825999,, InvoVac Canadian Model M8260027, and Vac ATS Model 8259968.

    FDA Recall
    Terminated ·KCI USA, Inc.·Product code OMP·November 4, 2009

    Fancy i Color cosmetic lens, Contents: A pair of sterile soft color contact lens immersed in buffered isotonic saline solution, Size: B.C. 8.6mm DIA. 14.5mm. Dreamcon Co. LTD. Korea.

    FDA Recall
    Terminated ·Kim's Trading Inc·Product code LPM·May 17, 2010

    PRE1001: Prevena Peel and Place System Kit Product Usage: The Prevena Incision Management System is intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed environment and removing exudates via the application of negative pressure wound therapy.

    FDA Recall
    Terminated ·KCI USA, INC.·Product code OMP·January 30, 2014

    CelluTome Epidermal Harvesting System Harvester (5.0 CM) STERILE EO Rx Only Manufactured for: KCI USA, Inc. Part Number CT-H50 or CT-H25 The CelluTome Epidermal Harvesting System is intended to reproducibly cut a thin skin graft for autologous skin grafting.

    FDA Recall
    Terminated ·KCI USA, INC.·Product code GFD·November 19, 2014

    500 mL InfoV.A.C. Canister (without Gel); Part #M8275071/5 (5 canister pack) and Part #M8275071/10 (10 canister pack); products are single use and labeled as STERILE; distributed by Kinetic Concepts, Inc., San Antonio, TX.

    FDA Recall
    Terminated ·KCI USA, Inc.·Product code JCX·July 29, 2008