BEUDAMED
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    Filters FDA Recall × Status: Terminated × Clear all

    Capnostream20 M NICU (CPM), CS08654RN

    FDA Recall
    Terminated ·Oridion Medical 1987 Ltd. Har Hotzvim Industrial·Product code DQA·July 31, 2018

    Capnostream20 M ADULT ICU (CPM), CS08654RA

    FDA Recall
    Terminated ·Oridion Medical 1987 Ltd. Har Hotzvim Industrial·Product code DQA·July 31, 2018

    PRO5100, PowerPro Battery Modular Handpiece. Drill mode Nominal Speed Range: 0-1250 rpm, PRO5200, PowerPro Battery Two Trigger Handpiece. Drill mode Nominal Speed Range: 0-1250 rpm, PRO5250, PowerPro Battery Two Trigger Handpiece. Drill mode Nominal Speed Range: 0-1250 rpm, PRO5300 PowerPro Battery Oscillator Handpiece. PRO 5300 Oscillator Speed Range: 0-11,000 cpm, and PRO5400 PowerPro Battery Reciprocator Handpiece. Speed Range: 0-14,500 cpm+/- 500 cpm. CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908 USA.

    FDA Recall
    Terminated ·Linvatec Corp. dba ConMed Linvatec·Product code HRX·July 31, 2009

    Bausch + Lomb Stellaris Elite 25 GA Vit Cutter, Model BL5628, 7500 cpm, packaged in sterile pouches, 6/shipper.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQE·August 8, 2018

    Bausch + Lomb Stellaris Elite 23 GA Vit Cutter, Model BL5627, 7500 cpm, packaged in sterile pouches, 6/shipper.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQE·August 8, 2018

    Bausch + Lomb Stellaris Elite 20 GA Vit Cutter, Model BL5626, 7500 cpm, packaged in sterile pouches, 6/shipper.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQE·August 8, 2018

    CDI Blood Parameter Monitoring System; Catalog Numbers or Part Numbers - 145891, 500AVHCT; Serial Numbers - BPM SN B015552 (installed into CDI 500 Monitor SN 3535)

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corporation·Product code DRY·May 9, 2014

    BIO-RAD 425-2020 Autoimmune EIA Anti-Cardiolipin IgM, 96 Tests...2010 02 16...Lot CL-863. Positive Control included in lot is identified as "REF 425-2025" and "LOT CPM-591". in vitro diagnostic.

    FDA Recall
    Terminated ·Bio-Rad Laboratories Inc·Product code DHC·July 14, 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

    RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage - Sinus Catheter - Intended to provide a means to access the sinus space for diagnostic and therapeutic procedures. .

    FDA Recall
    Terminated ·Acclarent, Inc.·Product code KAM·April 28, 2015

    - Relieva Flex Sinus Guide Catheter (Green) Tip Shape: F-70 Ref. GC070RF Lot 122429 - Relieva Luma Sentry 20 Tip Angle, 0.035 Diameter 100cm Ref. SIS100B Lot 122429 Manual surgical instrument for general use

    FDA Recall
    Terminated ·Surgical Instrument Service And Savings, Inc.·Product code KAM·May 3, 2013

    Accurus 2500 Standalone Vitreous Probe REF 8065741018; Accurus 23 GA Standalone Vitreous Probe REF 8065750821; Accurus 25+ 2500 CPM Standalone Vitreous Probe REF 8065751122; Anterior Accurus Probe with Infusion Needle REF 8065803650; Single Use Sterile Probes Rx only. Intended to provide the surgeon with a single-use probe for performing vitrectomy surgical procedures while using the Alcon Accurus vitrectomy console.

    FDA Recall
    Terminated ·Alcon Research, Ltd.·Product code HQC·June 2, 2015

    FLASH Ostial System, Dual Balloon Angioplasty Catheter, REF: OAB6014BA

    FDA Recall
    Terminated ·Ostial Corporation·Product code LIT·July 14, 2021

    RadiForce RX850, 8MP Color LCD Monitor, Part Code No. 0FTD1958A2, UPC 690592037180. This product is intended to be used in displaying and viewing digital images those of digital mammography for review and analysis by trained medical practitioners.

    FDA Recall
    Terminated ·Eizo Corporation 153 Shimokashiwano Hakusanshi Japan·Product code PGY·July 7, 2015

    Hospira brand Symbiq One-Channel Infuser; List Number: 16026; Distributed by: Hospira, Inc. Morgan Hill, CA and Manufactured by: Hospira Inc, La Aurora, Heredia, Costa Rica. Intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural or irrigation routes of administration.

    FDA Recall
    Terminated ·Hospira Inc·Product code FRN·April 9, 2010

    RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This product is intended to be used in displaying and viewing digital images including those of digital mammography for review and analysis by trained medical practitioners.

    FDA Recall
    Terminated ·Eizo Corporation 153 Shimokashiwano Hakusanshi Japan·Product code PGY·July 7, 2015

    Hospira brand Symbiq Two-Channel Infuser; List Number: 16027; Distributed by: Hospira, Inc. Morgan Hill, CA and Manufactured by: Hospira Inc, La Aurora, Heredia, Costa Rica. Intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural or irrigation routes of administration.

    FDA Recall
    Terminated ·Hospira Inc·Product code FRN·April 9, 2010

    InterGro DBM Demineralized Bone Matrix in a lipid carrier; Provided by: Lifelink Tissue Bank, Tampa, Florida, EBI A Biomet Company, Parsippany, New Jersey; REF DBM002. InterGro DBM product contain human tissue (allograft bpm) and are intended for transplantation. Products are to be used for filling bony voids or gaps in the extremities, and pelvis that are not intrinsic to the bony stability of the structure.

    FDA Recall
    Terminated ·Michigan Orthopaedic Products, Inc.·Product code MQV·May 5, 2008

    "***BIOMET MICROFIXATION***CENTER DRIVE STAINLESS STEEL***2.0MM SYSTEM SCREWDRIVER BLADE***Non-Sterile Product***BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com***" Blade used to implant screws.

    FDA Recall
    Terminated ·Biomet Microfixation, Inc.·Product code LXH·March 15, 2010

    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135417

    FDA Recall
    Terminated ·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010