FDA recall Z-0241-2023

Steris Corporation · Class II · device

Product

GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to perform cutting and/or coagulation and coagulation with or without delivery of argon gas, in flexible endoscopic applications. MODEL #(s): G1110001

Reason for recall

Two electronic diode components (D1 & D4) placed in the reverse orientation on the controller printed circuit board assembly may result in premature wear of the power regulator, leading to the regulators failure which could cause a full power loss. If the regulator failure were to occur during a patient procedure, a procedural delay may result

Distribution

US Nationwide distribution in the states of Arizona, Illinois, Tennessee, Virginia.

Key facts

Status
Terminated
Initiation date
2022-10-17
Report date
2022-11-23
Termination date
2024-05-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mentor, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0241-2023