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Video Bronchoscope

FDA Recall
Terminated ·Pentax of America Inc·Product code EOQ·January 11, 2011

Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and therapeutic access to, the biliary tract via the upper GI tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: esophagus, stomach, duodenum, common bile, hepatic and cystic ducts.

FDA Recall
Terminated ·Pentax of America Inc·Product code FDT·January 17, 2017

C2 CryoBalloon Controller, REF: FG-1017, with Controller Software v1.18.258 The C2 CryoBalloon Ablation System is intended to be used as a cryosurgical tool in the field of general surgery, specifically for endoscopic application and the ablation of dysplastic Barrett s Esophagus.

FDA Recall
Terminated ·PENTAX of America Inc·Product code GEH·December 3, 2018

Pentax Video Colonoscope Model: EC38-i10L

FDA Recall
Terminated ·Pentax of America Inc·Product code FDF·January 3, 2020

Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models: EG-2790i, EG-1690K, EG-2490K, EG-2790K, EG27-i10; Gastroscope Family # 2- Gastroscopes with a Water Jet Channel Models: EG-2990i, EG-2990K, EG-3490K, EG29-i10; Gastroscope Family # 3-Gastroscopes with Two Instrument Channels and a Water Jet Channel Models: EG-3890TK

FDA Recall
Open, Classified ·Pentax of America Inc·Product code FDF·July 14, 2021

Ultrasound Video Gastroscope, Model EG-3870UTK. The product is intended to be used in combination with the ultrasound scanning unit made by Hitachi Medical Corporation, and the PENTAX Medical video processor to provide images for observation, diagnosis, imaging, or therapy of the upper gastrointestinal tract from esophagus through duodenum.

FDA Recall
Terminated ·Pentax of America Inc·Product code ODG·May 23, 2017

9400 Laryngeal Strobe Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of laryngeal or pharyngeal structures, and audio data, for medical and pedagogical applications.

FDA Recall
Terminated ·Pentax of America Inc·Product code GCW·April 13, 2017

Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One Instrument Channel and a Water Jet Channel Models: EC-2990Li, EC-3490Li, EC-3890Li, EC-3490TLi, EC-3490LK, EC-3890LK, EC3890LZi, EC34-i10L, EC38-i10L; Colonoscope Family # 2-Pentax Video Colonoscopes with Two Instrument Channels and a Water Jet Channel Model: EC-3890TLK

FDA Recall
Open, Classified ·Pentax of America Inc·Product code FDF·July 14, 2021

Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are intended to provide optical visualization of (via a video monitor), and therapeutic access to, the biliary tract via the upper GI tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: esophagus, stomach, duodenum, common bile, hepatic, and cystic ducts.

FDA Recall
Terminated ·Pentax of America Inc·Product code FDT·February 13, 2018

Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecare Bed containing the Okin Dumat 3 Head/Foot Motors. Description Part Number Motor and Pendant Patriot Full Electric 120V 690-3001-943 / 690-7001-943 Boxed Full Electric 220V Motor 690-3220-943 Motor and Pendant Patriot LX Full Electric 120V 690-8004-912

FDA Recall
Terminated ·GF Health Products, Inc·Product code FNL·September 30, 2016

9310HD Digital Video Capture Modules Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of laryngeal or pharyngeal structures, and audio data, for medical and pedagogical applications.

FDA Recall
Terminated ·Pentax of America Inc·Product code GCW·April 13, 2017

9310HD Digital Video Capture Module with software version 3.4.0 or higher configured with 9263 endoPortal

FDA Recall
Terminated ·Pentax of America Inc·Product code OUG·September 22, 2020

Video Cystoscope models ECY-1570 and ECY-1570K

FDA Recall
Terminated ·Pentax of America Inc·Product code FAJ·July 13, 2017

Video Cytoscopes

FDA Recall
Terminated ·Pentax of America Inc·Product code EOQ·January 11, 2011

Video Naso pharyngo Laryngoscopes

FDA Recall
Terminated ·Pentax of America Inc·Product code EOQ·January 11, 2011

Pentax Medical C2 CryoBalloon Pear Focal Catheter, Model FG 1024, Sterile, RX. Product Usage: The C2 CryoBalloon Ablation System is intended to be used as a cryosurgical tool in the field of general surgery, specifically for endoscopic application and the ablation of dysplastic Barrett s Esophagus. The system includes the following components: (1) CryoBalloon Catheter connects to the Controller, which controls the operation of the Catheter such as diffuser (sprayer) positioning and ablation (nitrous oxide release); (2) CryoBalloon Controller contains the cartridge heater and cryogen delivery valve, which is controlled with the foot pedal; (3) Foot Pedal; and (4) CryoBalloon Cartridge containing 36 grams of nitrous oxide.

FDA Recall
Terminated ·PENTAX of America Inc·Product code GEH·December 3, 2018

Fungitell STAT- IVD Assay for (1 3)-~-D-Glucan in Serum Ref: FT007

FDA Recall
Terminated ·Associates of Cape Cod, Inc.·Product code NQZ·August 17, 2022

Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement. Do not reuse. Ethylene Oxide Sterilized. Made in the U.S.A. Synovis Surgical Innovations A division of Synovis Life Technologies, Inc., 2575 University Ave. W., St. Paul, MN 55114-1024 USA.

FDA Recall
Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·November 1, 2005

i-STAT EG7+ Cartridge; pH, PCO, PO, Na , K, iCa, Hct. Test include: Electrode Measurement Blood-Gases (Pco2, PO2) and Blood Ph, Electrode, Ion Specific, Potassium, Electrode, Ion Specific, Calcium, Electrode, ion Specific, Sodium and Hematocrit. Catalog number 220300. Abbott Point of Care inc., Abbott Park, IL 60064 USA Intended use is to quantify measurement of sodium, potassium, ionized calcium, oxygen, carbon dioxide, pH and Hematocrit in blood.

FDA Recall
Terminated ·Abbott Point of Care Inc.·Product code CHL·February 23, 2009

i-STAT CK-MB cartridge Abbott Point of Care, Princeton, NJ 08540

FDA Recall
Terminated ·Abbott Point Of Care Inc.·Product code CHL·January 1, 2008