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US Endoscopy Group Recalls
10 recalls on record · September 26, 2012 to March 20, 2019 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 20, 2019Medical DevicesFDA
US Endoscopy Group Inc recalls US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endo
Hazard: Potential esophageal laceration during a patient procedure
March 15, 2017Medical DevicesFDA
US Endoscopy Group Inc recalls Roth Net Polyp Retrieval
Hazard: The firm was notified that the expiration date on the outer carton is different than the expiration date on the inner package. The expiration date is shorter than the actual expiration.
October 26, 2016Medical DevicesFDA
US Endoscopy Group Inc recalls Vari-Safe Injection Needle US endoscopy 5976 Heisley Road Mentor, Ohio 44060 A sterile, single use, flexible sheath d
Hazard: US Endoscopy is conducting a voluntary product recall of one lot of the Vari-Safe Injection Needle as it was identified that the lot was incorrectly distributed. The lot was assembled with internal catheter components which differ from the original Vari-Safe needle internal catheter components. All components are dimensionally similar to the original Vari-Safe needle internal catheter components and the components have history of use on other US Endoscopy needle products.
October 7, 2015Medical DevicesFDA
US Endoscopy Group Inc recalls Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp, dis
Hazard: The company has determined the sterility cannot be assured for the affected lot.
July 8, 2015Medical DevicesFDA
US Endoscopy Group Inc recalls Velocity" Biopsy Valve, 25 units per box, Product Usage: The disposable Velocity biopsy valve is used to cover the
Hazard: The company has received reports of structural non conformance at the connection between the valve body and the irrigation tube, resulting in separation of the components during use.
April 22, 2015Medical DevicesFDA
US Endoscopy Group Inc recalls Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi
Hazard: A wire component on the distal grasping assembly of the device became detached..
December 31, 2014Medical DevicesFDA
US Endoscopy Group Inc recalls UroSeal Adjustable Endoscopic Valve. Model/Catalog # 00913410 The primary packaging is a Tyvek pouch. The secondary p
Hazard: Packaging non-conformance related to the integrity of the sterile pouch seal.
April 17, 2013Medical DevicesFDA
US Endoscopy Group Inc recalls Torrent" irrigation tubing. Product Usage: The Torrent irrigation system (tubing and accessories to accommodate
Hazard: The firm was notified by their customers that there was a water leakage from the white tubing connector.
October 10, 2012Medical DevicesFDA
US Endoscopy Group Inc recalls Endoscopic retrieval device. The disposable Raptor grasping device in intended to retrieve foreign bodies or resected
Hazard: When the outer catheter is either coiled or in a contorted configuration outside of the endoscope and the patient, and excessive force is applied to the handle, the jaws may become inoperable and may become stuck in the open condition.
September 26, 2012Medical DevicesFDA
US Endoscopy Group Inc recalls Infinity¿ sampling device, Cytology Brush, United States Endoscopy Group, Inc., 5976 Heisley Road, Mentor, OH 44060 T
Hazard: US Endoscopy received five complaints which noted difficulty in deploying the cytology brush through the catheter.