Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2213-2013 — Responder 5 is a nurse call communication system that connects patients with staff in a hospital. The nurse call system also connects team members and departments from radiology, physical therapy, transport, environmental services and more. Responder 5 is used in hospitals and long term pati

U.S. FDA — Device Enforcement · United States · 2013-05-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2213-2013
Date of alert
2013-05-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Rauland-Borg Corp
Product category
device
Product type
Devices
Reported risk: A counterfeited electronic component was identified in the products affected. The component, a data transceiver (transmitter/receiver), is associated with the intercommunication of these devices in the Responder 5 system across the L-Net data path. Failure of a data transceiver results in the loss of nurse call functionality in the associated room, and may disrupt communications on the L-Net run
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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