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CDLCAM, First-Pass Radionuclide Angiography Camera System, Model 70-500101, with operating Software Version B1A, marketed by CDL Medical Tech.

FDA Recall
Terminated ·GVI Technology Partners·Product code IYX·January 16, 2004

PRN 50-M+, GE part number 2062759-001, manufacturer part number 600-23310-01 Product Usage: The PRN 50M+ Paper Chart Recorder thermally records patient data on a paper strip. This device is intended for use under direct supervision of a licensed health care practitioner. This device is not intended for home use.

FDA Recall
Terminated ·Gsi Group Inc·Product code DSF·December 2, 2015

PRN 50-M+, GE part number 2062759-001, manufacturer part number 600-23310-01 Product Usage: The PRN 50M+ Paper Chart Recorder thermally records patient data on a paper strip. This device is intended for use under direct supervision of a licensed health care practitioner. This device is not intended for home use.

FDA Enforcement
Class II ·Terminated·Gsi Group Inc·March 2, 2016

Empi STIMC RE Self Adhesive electrodes. For use on TENS, NMES, FES. a DJO brand A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., electroencephalogram) or to apply electrical stimulation.

FDA Recall
Terminated ·Covidien LLC dba Uni-Patch·Product code GXY·February 9, 2012

Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes, A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., electroencephalogram) or to apply electrical stimulation.

FDA Recall
Terminated ·Covidien LLC dba Uni-Patch·Product code GXY·February 9, 2012

Reusable, Self-Adhering TENS/NMES/FES electrodes Single Patient Use Only. An electrocardiograph electrode is the electrical conductor which is applied to the surface of the body to transmit the electrical signal at the body surface to a processor that produces an electrocardiogram or vectorcardiogram.

FDA Recall
Terminated ·Covidien LLC dba Uni-Patch·Product code GXY·February 9, 2012

Reusable, non-sterile, self-adhering electrodes for use with TENS/NMES, . Made in the U.S.A. Cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.

FDA Recall
Terminated ·Covidien LLC dba Uni-Patch·Product code GXY·February 9, 2012

Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes, A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., electroencephalogram) or to apply electrical stimulation.

FDA Enforcement
Class II ·Terminated·Covidien LLC dba Uni-Patch·December 19, 2012

Empi STIMC RE Self Adhesive electrodes. For use on TENS, NMES, FES. a DJO brand A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., electroencephalogram) or to apply electrical stimulation.

FDA Enforcement
Class II ·Terminated·Covidien LLC dba Uni-Patch·December 19, 2012

Reusable, non-sterile, self-adhering electrodes for use with TENS/NMES, . Made in the U.S.A. Cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.

FDA Enforcement
Class II ·Terminated·Covidien LLC dba Uni-Patch·December 19, 2012

Reusable, Self-Adhering TENS/NMES/FES electrodes Single Patient Use Only. An electrocardiograph electrode is the electrical conductor which is applied to the surface of the body to transmit the electrical signal at the body surface to a processor that produces an electrocardiogram or vectorcardiogram.

FDA Enforcement
Class II ·Terminated·Covidien LLC dba Uni-Patch·December 19, 2012

Large Volume Paracentesis Kit is packaged in a thermaformed tray which contains slots and snap-in holders for most components. Packed sterile in Tyvek bag. Catalog #: GIS-28 Lot #: 61442434 Expiration Date: 2018/04

FDA Enforcement
Class II ·Terminated·Gi Supply·March 16, 2016

Lingen SAMPLE Disposable Virus Sampling Kit pack, Item SAM ENI MTM-04, containing 2 tubes and 2 swabs/pack; and SAM ENI MTM04TUBE, containing 1 tube/pack.

FDA Recall
Terminated ·Mercedes Medical, Inc.·Product code QBD·June 10, 2021

Lingen SAMPLE Disposable Virus Sampling Kit pack, Item SAM ENI MTM-04, containing 2 tubes and 2 swabs/pack; and SAM ENI MTM04TUBE, containing 1 tube/pack.

FDA Enforcement
Class II ·Terminated·Mercedes Medical, Inc.·July 21, 2021

Crosslock DVR ePAK -Sterile, Ref 81180050, are complete surgical sets including plates, screws, and instruments for orthopedic fixation The Cross lock DVR ePAK Volar Rim Plates system is intended for fixation of fractures, mal unions, and osteotomies involving the distal radius. The DVR Wrist ePAK system is intended stabilization and fixation of small bone fragments in fresh fractures, revision procedures, joint fusion and reconstructions of small bones of the hand, foot, radius, ulna, ankle, humerus, scapula and pelvis, particularly in osteopenic bone.

FDA Enforcement
Class II ·Terminated·Biomet, Inc.·March 16, 2016

PM1000 Flow Selector - An accessory to an emergency ventilator (resuscitator). The selector is attached to a flowmeter and is used to direct the outlet flow from any standard flowmeter to any one of the three outlets it provides.

FDA Recall
Terminated ·Precision Medical, Inc.·Product code BTM·March 5, 2010

PENTAX Upper/Lower G.I. Endoscope OF-B130 and OF-B194 Gas/Water Feeding Valve

FDA Recall
Terminated ·Pentax Medical Company·Product code KOG·July 17, 2014

Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00 used with ER920 Wireless Series Arrhythmia Event Recorder. Non-rechargeable disposable battery pack.

FDA Enforcement
Class II ·Terminated·BRAEMAR, INC.·July 10, 2013

Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-01 used with ER920 Wireless Series Arrhythmia Event Recorder. Non-rechargeable disposable battery pack.

FDA Enforcement
Class II ·Terminated·BRAEMAR, INC.·July 10, 2013

Freedom EV0-2 with any version of EVOware and EVOware Sample Tracking Add-On V1.0 or higher

FDA Recall
Terminated ·Tecan US, Inc.·Product code JQW·July 23, 2018