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easyEndoTM Universal Linear Cutting Stapler and Loading Units for Single Use

Ezisurg Medical Co., Ltd. · Model R45C · UDI-DI 06925776123491

GDW Prescription
1
510(k) clearances
171,420
Adverse events (1,104 deaths)
225
Recalls
154
Facilities

Description

Loading Units, 45±2mm Long, 3.8±0.2mm height, gold

Recalls

DateFirmReason
2025-09-25Covidien, LPA manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
2025-09-25Covidien, LPA manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
2025-09-11Ethicon Endo-Surgery IncThe devices were shipped unsterilized.
2025-04-22Ethicon Endo-Surgery IncFirm has received an increase in reports regarding inadvertent instrument lockout during surgical procedures involving the device. If lockout occurs, the device will momentarily ac
2024-08-12Smith & Nephew Inc.Product packaging process may result in an improper or incomplete seal of the outer foil pouch surrounding the inner Tyvek pouch, compromising product sterility
2024-08-12Smith & Nephew Inc.Product packaging process may result in an improper or incomplete seal of the outer foil pouch surrounding the inner Tyvek pouch, compromising product sterility
2024-04-15Covidien, LPPotential damage to the cartridge can result in poor staple formation and/or incomplete staple line, may cause a delay in surgery
2024-02-14Covidien, LPUnder certain firing conditions, reloads were found to articulate in an uncontrolled manner potentially causing disruption to the staple line. The issue is related to components in
2024-02-14Covidien, LPUnder certain firing conditions, reloads were found to articulate in an uncontrolled manner potentially causing disruption to the staple line. The issue is related to components in
2023-12-11Ethicon Endo-Surgery IncThere is the potential for incomplete staple line formation during the firing sequence, without most or all staples, which may lead to insufficient tissue apposition that could req

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.