RecallRadar

FDA Device recall Z-2213-2013

Responder 5 is a nurse call communication system that connects patients with staff in a hospital

On 2013-09-25 the FDA classified a Class II recall of Responder 5 is a nurse call communication system that connects patients with staff in a hospital by Rauland Borg, citing A counterfeited electronic component was identified in the products affected. The component, a data transceiver (transmitter/receiver), is associated with the intercommunication o….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2213-2013
ClassificationClass II
Statusterminated
Initiated2013-05-10
Published2013-09-25
Last updated2026-09-13 11:53 UTC
CompanyRauland Borg
DistributionUS

Product

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 patient care facilities to allow for remote communications between patients and patient monitoring devices and healthcare providers

Reason

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

Identifiers

code_info1) Product Code 351000 (Branch Regional Controller); 2) Product Code 352000 (Corridor Light); 3) Product Code 352020 (Domeless Controller)

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2213-2013%22

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