39 results
·
11ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Terminated
×
Fischer Cone Biopsy Excisor - Lg - Shallow Model: 900-155
FDA Recall
Terminated
·Apple Medical Corporation·Product code HGI·March 10, 2006
Quantam 2000 Electrosurgical Generator, Part number 909075-05.
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code HGI·October 16, 2019
Fischer Cone Biopsy Excisor Model: 900-158
FDA Recall
Terminated
·Apple Medical Corporation·Product code HGI·March 10, 2006
Fischer Cone Biopsy Excisor - Small Model: 900-150
FDA Recall
Terminated
·Apple Medical Corporation·Product code HGI·March 10, 2006
CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D, 12 cm shaft ). Box of 5 Model Number(s): R2010 Intended Use: Diagnosis and treatment of non-invasive HPV-related or unrelated lesions of the lower genital tract.
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code HGI·October 27, 2014
Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code HGI·March 12, 2018
Fischer Cone Biopsy Excisor - Medium Model: 900-151
FDA Recall
Terminated
·Apple Medical Corporation·Product code HGI·March 10, 2006
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code HGI·June 18, 2019
Quantam 2000 Electrosurgical Generator, Part number 909075.
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code HGI·October 16, 2019
Fischer Cone Biopsy Excisor - Medium - Ext Model: 900-154
FDA Recall
Terminated
·Apple Medical Corporation·Product code HGI·March 10, 2006
Sterile, single-use, disposable electrosurgical electrode holder. It connects the electrode to the foot activated electric generator. Label reads in part "***GYNEX*** Electrode Handpiece, Foot Activated*** Manufactured for GYNEX***" Gynex catalog number: 950 (Gynex REF 950, Electrode Handpiece) It connects the electrode to the food activated electric generator. Electrodes are used in gynecological procedures, in a physician's office, for cutting to remove tissue and coagulation to control bleeding by the use of high frequency current.
FDA Recall
Terminated
·Gynex Corporation·Product code HGI·September 6, 2012
Fischer Cone Biopsy Excisor Model: 900-157
FDA Recall
Terminated
·Apple Medical Corporation·Product code HGI·March 10, 2006
Fischer Cone Biopsy Excisor - Dual Sets Model: 900-156
FDA Recall
Terminated
·Apple Medical Corporation·Product code HGI·March 10, 2006
Quantam 2000 Electrosurgical Generator, Part number 909075-05W.
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code HGI·October 16, 2019
Fischer Cone Biopsy Excisor - Large Model: 900-152
FDA Recall
Terminated
·Apple Medical Corporation·Product code HGI·March 10, 2006
LEEP Precision Integrated System 120V, Model LP-10-120 Product Usage: The LEEP PRECISION INTEGRATED SYSTEM l 20V combines three components - LEEP PRECISION Cart, LEEP PRECISION Generator, and the LEEP PRECISION Smoke Evacuator for loop electrosurgical excision procedures. The loop electrosurgical excision procedure (LEEP) utilizes a very thin wire in the shape of a loop heated by electrical current generated by a power supply to efficiently remove abnormal cells. The LEEP PRECISION INTEGRATED SYSTEM has been designed to provide an efficient workstation that can efficiently meet all the unique LEEP requirements of the clinic and practice-based facilities .
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code HGI·April 23, 2019
Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115) - Primary packaging is 12 pouches with Tyvek header (10.75 x 16.375 x 3") within a secondary corrugated shipper (20.75 x 15.50 x 8.5" inner dimensions). The device is intended to be connected to a powered breast pump or adapted for use with a manual breast pump to express and collect the mother's milk of a nursing woman for the purpose of feeding the collected milk to a baby.
FDA Recall
Terminated
·Ameda, Inc.·Product code HGY·February 12, 2015
Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging is 6 pouches with Tyvek header (9.5 x 13.63 x 3.75") within a secondary corrugated shipper (16 x 11.02 x 5.12" inner dimensions). The device is indicated for assisted expression of milk using manual suction.
FDA Recall
Terminated
·Ameda, Inc.·Product code HGY·February 12, 2015
Multitom RAX with software version VF10
FDA Enforcement
Class II
·Terminated·Siemens Medical Solutions USA, Inc·June 9, 2021
Multitom RAX with software version VF10
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code OWB·April 20, 2021