Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac EPF/EGR Hook Blade, Angled, Catalog Number 3055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac ECTR Triangle Blade, Angled, Catalog Number 2054A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endintrak¿ 2 Hook Blade, Angled, Catalog Number 4058A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac ECTR Hook Blade, Angled, Catalog Number 2055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac ECTR Triangle Blade, Catalog Number 2054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac ECTR Push Blade, Catalog Number 2053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac ECTR Hook Blade, Catalog Number 2055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrig ETF Hook Blade, Catalog Number 1052-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac EPF/EGR Triangle Blade, Catalog Number 3054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Stryker GmbH - Endotrig, Endotrac and Endintrack Blade Kits - Class 2 Recall
Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 29, 2019 Category: Medical Devices Source Type: alerts

Agfa N.V. - AGFA Digital Radiography X Ray system DR 800 - Class 2 Recall
AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Product Usage: The Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following an anatomies/procedures: positioning fluoroscopy procedures, gastro-intestinal examinations, urogenital tract examinations, and angiography. It is intended to replace fluoroscopic images obtained through image intensifier technology. In addition, the system is intended for project radiography of all body parts. The DR 800 is not intended for mammography applications. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 31, 2019 Category: Medical Devices Source Type: alerts

Medline Industries Inc (Northpoint Services) - Antifog solution - Class 2 Recall
Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows: ROBOTIC GENERAL, LAP CHOLE, GENERAL LAPAROSCOPY PACK-LF, T&A PACK, LAP CHOLE PACK-LF, LAPAROSCOPY PACK-LF, EAR ACCESSORY PACK, RF LAP CHOLEPACK (LCLUI)642-LF, GEN LAPAROSCOPY PACK-LF, LAPAROSCOPY PELVISCOPY PACK, LAP ABDOMINAL CDS-LF, GENERAL LAPAROSCOPY CDS, GYN LAPAROSCOPY CDS, CSMC/ENDOSINUS/NASAL PACK-LF, GENERAL LAPAROSCOPY PACK, GENERAL SURGERY, MODULE TONSIL, MODULE GYN LAP NATALIE, GEN SURGERY LAP CHOLE PACK, T & A CDS, GYN LAPAROSCOPY PACK, GENERAL LAPAROSCOPY, GYN LAPAROSCOPY, TONSIL PACK, LAPA...
Source: Medical Device Recalls - July 19, 2019 Category: Medical Devices Source Type: alerts

Philips Medical Systems (Cleveland) Inc - Vereos PET/CT - Class 2 Recall
Vereos PET/CT, Model No. 882446 Product Usage: Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem images anatomical cross-sections by computer reconstruction of X-ray transmission data. The PET subsystem images the distribution of PET anatomy-specific radiopharmaceuticals in the patient. The PET/CT system is used for the purposes of detecting, localizing, diagnosing, staging, re-staging, and follow-up for monitoring therapy response of various diseases in oncology, cardiology, and neurology. The system is intended to image the whole body, heart, brain, lung, gastrointestinal, b...
Source: Medical Device Recalls - July 4, 2019 Category: Medical Devices Source Type: alerts

Luminex Molecular Diagnostics - xTAG Gastrointestinal Pathogen Panel (GPP) Kit - Class 2 Recall
xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple viral, bacterial and parasitic nucleic acids in human stool specimens or human stool (GPP) Kit, IVD, REF I032C0316. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 11, 2019 Category: Medical Devices Source Type: alerts