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Snare, Non-Electrical

FDA product code FGX · Class 1 · Gastroenterology, Urology

74
Registered devices
572
Adverse events
47
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-10-24Endo-Therapeutics, Inc.Improper device regulatory classification
2021-10-29Diversatek HealthcareM-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were shipped between 9-27-2021 and 10-22-2021, may contain incorrect inner polybag labelin
2021-01-04Aomori Olympus Co., Ltd.Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equ
2021-01-04Aomori Olympus Co., Ltd.Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equ
2021-01-04Aomori Olympus Co., Ltd.Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equ
2021-01-04Aomori Olympus Co., Ltd.Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equ
2021-01-04Aomori Olympus Co., Ltd.Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equ
2021-01-04Aomori Olympus Co., Ltd.Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equ
2021-01-04Aomori Olympus Co., Ltd.Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equ
2021-01-04Aomori Olympus Co., Ltd.Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equ

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.