392 results
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17ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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NEEDLEMASTER 3MMx 23G LOWER, model no. NM-610L-0523 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code FBK·January 4, 2021
NEEDLEMASTER 6MMx 25G LOWER, model no. NM-610U-0625 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code FBK·January 4, 2021
NEEDLEMASTER 3MMx 23G LOWER, model no. NM-610U-0323 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code FBK·January 4, 2021
Vari-Safe Injection Needle US endoscopy 5976 Heisley Road Mentor, Ohio 44060 A sterile, single use, flexible sheath device intended to be used for the injection of various types of media through flexible endoscopes
FDA Recall
Terminated
·US Endoscopy Group Inc·Product code FBK·May 18, 2016
NEEDLEMASTER 6MMx 23G UPPER, model no. NM-610L-0623 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code FBK·January 4, 2021
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
NEEDLEMASTER 4MMx 21G UPPER, model no. NM-610L-0421 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code FBK·January 4, 2021
NEEDLEMASTER 1.8MMx 26G LOWER, model no. NM-610U-1826 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code FBK·January 4, 2021
NEEDLEMASTER 4MMx 25G UPPER, model no. NM-610L-0425 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code FBK·January 4, 2021
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Enteryx Injector Single Pack Order Number: M00572650-US and M00572630 -OUS
FDA Recall
Terminated
·Boston Scientific Corporation·Product code FBK·September 23, 2005
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Hobbs Posi-Stop Injection Needle Catalog Number: 4718
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·July 29, 2022
Hobbs Posi-Stop Injection Needle Catalog Number: 4722
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·July 29, 2022
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Hobbs Posi-Stop Injection Needle Catalog Number: 4720
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·July 29, 2022
ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early-stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device UPN: (1)Twin Pack Box 1 M00519210; (2)Twin Pack Box 10 M00519211; (3)Single Pack Box 10 M00519231
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FBK·October 10, 2022
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Acuject Variable Injection Needle
FDA Recall
Terminated
·Wilson-Cook Medical Inc.·Product code FBK·June 14, 2019