BEUDAMED
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    CARA (Computer Assisted Retinal Analysis), Product ID: +B543CARA0/$$+7V4.7.2/16D202111179

    FDA Recall
    Terminated ·Diagnos Inc·Product code NFJ·January 11, 2022

    ORA System with VerifEye, Catalog Number 8065998300 For use during intraocular lens surgery

    FDA Recall
    Terminated ·Alcon Research, Ltd.·Product code NCF·June 30, 2017

    ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery

    FDA Recall
    Terminated ·Alcon Research, Ltd.·Product code NCF·June 30, 2017

    Healing Labs Rite Choice Pregnancy Test Kit, packed in a cellophane display box, containing one test strip and materials for one test, and labeled in part ***Distributed by Core Brands, 1301 Wicomico St Baltimore, MD 21230 USA***Made in China***UPC 087399430205***. Packed 48 boxes/case.

    FDA Recall
    Terminated ·Core Brands·Product code LCX·June 22, 2005

    Medtronic brand KyphX HV-R Bone Cement, a polymethyl bone cement consisting of a quantity of powder (20 g) and a volume of liquid (10 ml/9 g) mixed in a Kyphon mixer for up to two minutes. Model Number: CO1A; Manufactured by Elmdown LTD, London, England, for Medtronic Spine LLC, Sunnyvale, CA. Product is a medical device used during balloon kyphoplasty to cement structures in fractured vertebral bodies.

    FDA Recall
    Terminated ·Medtronic Spine LLC, formerly Kyphon Inc·Product code NDN·November 10, 2009

    Dow Corning Silastic brand Medical Adhesive Silicone, Type A, non-sterile, 57 gram tube; material numbers 3242901 (100 tubes) and 3242897 (6 tubes).

    FDA Recall
    Terminated ·Dow Corning Corp.·September 5, 2003

    One Touch Basic/Profile and One Touch Ultra Blood Glucose Test Strips

    FDA Recall
    Terminated ·Core Care Technologies, Inc·Product code NBW·October 14, 2006

    PrestiBio BREAST MILK ALCOHOL TEST STRIP REF 910-10 25 TESTS

    FDA Recall
    Open, Classified ·Universal Meditech Inc.·Product code ORA·May 22, 2023

    Alcon Clareon IOL with AutonoMe Delivery System

    FDA Recall
    Terminated ·Alcon Laboratories Ireland, Ltd Cork Business And Technology Park Model Farm Road Cork Ireland·Product code HQL·May 11, 2022

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 3 CEM. Part Number: 150450203.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.

    FDA Recall
    Open, Classified ·DEPUY (IRELAND) Loughbeg, Ringaskiddy Co. Cork Ireland·Product code KRO·April 3, 2026

    Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concentrators are non-sterile, disposable, multiwall ultrafiltration devices. Minicon clinical sample concentrators are for in vitro diagnostic use and are intended for concentrating serum, urine, cerebrospinal fluid, and other body fluids prior to analysis.

    FDA Recall
    Terminated ·Merck Millipore Ltd. Tullagreen Carrigtwohill County Cork Ireland·Product code JJH·May 14, 2018

    BIOSTOP G BIORESORBABLE CEMENT RESTRICTOR Catalog Numbers: 546308000 (Size 8); 546310000 (Size 10); 546312000 (Size 12); 546314000 (Size 14); 546316000 (Size 16); 546318000 (Size 18); 546320000 (Size 20)

    FDA Recall
    Open, Classified ·Depuy Ireland UC Loughbeg, Ringaskiddy Co. Cork Munster Ireland·Product code LZN·December 19, 2022