GASTROPAR (gentiana lutea, sambucus nigra, stomach (suis), symphytum officinale, arsenicum album, bismuthum subnitricum, carbo vegetabilis, lycopodium clavatum, nux vomica, phosphorus) liquid [Energique, Inc.]
Updated Date: Tue, 03 Aug 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - August 3, 2021 Category: Drugs & Pharmacology Source Type: alerts
GASTROCROM (cromolyn sodium) liquid [Meda Pharmaceuticals]
Updated Date: Thu, 15 Jul 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - July 15, 2021 Category: Drugs & Pharmacology Source Type: alerts
Pentax of America Inc - Class 2 Recall
Pentax Medical Video Duodenoscope - Product Usage: intended to be used with endoscopic devices and other ancillary equipment to provide optical visualization of (via a video monitor), and therapeutic access to, Biliary Tract via the Upper Gastrointestinal Tract, Model Number: ED34-i10T2. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 26, 2021 Category: Medical Devices Source Type: alerts
Covidien Llc - Bravo pH and CF Capsule - Class 2 Recall
BRAVO PH CAPS DELIVERY DEV5-PK, FGS-0312/FGS-0313 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 2, 2021 Category: Medical Devices Source Type: alerts
Covidien Llc - Bravo pH and CF Capsule - Class 2 Recall
CF Delivery Dev Caps Bravo x5, FGS-0635/FGS 0636 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 2, 2021 Category: Medical Devices Source Type: alerts
Hollister Incorporated - Vertical Drain Tube Attachment Device (VTAD) - Class 2 Recall
Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to stabilize and secure a variety of catheters, surgical drains, and tubes from sizes 5-40 French. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 27, 2021 Category: Medical Devices Source Type: alerts
Northgate Technologies, Inc. - Steris CO2MPACT Endoscopic Insufflator - Class 2 Recall
Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2 as a distention media in the gastrointestinal tract when used in conjunction with a gastrointestinal endoscope. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 25, 2021 Category: Medical Devices Source Type: alerts
Cairn Diagnostics - 13CSpirulina Gastric Emptying Breath Test - Class 2 Recall
13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended for use in the measurement of the rate of gastric emptying of solids and as an aid in the diagnosis of delayed gastric emptying (gastroparesis) in adult humans who are symptomatic for gastroparesis. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 17, 2021 Category: Medical Devices Source Type: alerts
Aomori Olympus Co., Ltd. - INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM - Class 2 Recall
INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM, model no. NM-400L-0421 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2021 Category: Medical Devices Source Type: alerts
Aomori Olympus Co., Ltd. - INJECTOR FORCEMAX LOWER 23G 6MM 5/BX - Class 2 Recall
INJECTOR FORCEMAX LOWER 23G 6MM 5/BX, model no. NM-400U-0623 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2021 Category: Medical Devices Source Type: alerts
Aomori Olympus Co., Ltd. - INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM - Class 2 Recall
INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM, model no. NM-400L-0625 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2021 Category: Medical Devices Source Type: alerts
Aomori Olympus Co., Ltd. - INJECTOR FORCEMAX SIF 270CM 23G 4MM - Class 2 Recall
INJECTOR FORCEMAX SIF 270CM 23G 4MM, model no. NM-401L-0423 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2021 Category: Medical Devices Source Type: alerts
Aomori Olympus Co., Ltd. - INJECTOR FORCEMAX UP 2.8MMCH 23G 4MM - Class 2 Recall
INJECTOR FORCEMAX UP 2.8MMCH 23G 4MM, model no. NM-400L-0423 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2021 Category: Medical Devices Source Type: alerts
Aomori Olympus Co., Ltd. - INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM - Class 2 Recall
INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM, model no. NM-400L-0621 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2021 Category: Medical Devices Source Type: alerts
Aomori Olympus Co., Ltd. - INJECTOR FORCEMAX LOWER 23G 3MM - Class 2 Recall
INJECTOR FORCEMAX LOWER 23G 3MM, model no. NM-400U-0323 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2021 Category: Medical Devices Source Type: alerts
