Nihon Kohden recalls specific WMTS Telemetry Receivers due to incorrect date stamps or no data transfer. Affected models include ORG 9100A, 9110A, and 9700A with specific serial numbers. Consumers should check their device details.
Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.
Nihon Kohden is recalling certain WMTS Telemetry Receivers that may have incorrect date stamps or fail to transfer data. This could lead to inaccurate patient monitoring readings, which might affect medical care decisions.
The receivers may show incorrect dates or fail to transfer patient data. This could result in improper medical decisions if healthcare providers rely on the device for monitoring.
Healthcare providers using the recalled telemetry receivers are most at risk. Patients using these devices for monitoring may experience inaccurate readings.
Check for model numbers ORG 9100A, ORG 9110A, or ORG 9700A with specific serial numbers listed in the recall notice. The recall covers devices sold with certain serial number ranges.
Identify the model number and serial numbers on your WMTS Telemetry Receiver to see if it matches the recalled units.
The recall affects WMTS Telemetry Receivers with model numbers ORG 9100A, ORG 9110A, and ORG 9700A, and specific serial number ranges.
No immediate stop is required. The recall does not specify a need to stop using the device, only to check if it is affected.
Check the model number and serial numbers against the list provided in the recall notice: ORG 9100A serial numbers 00001-01413, ORG 9110A serial numbers 00001-02706, ORG 9700A serial numbers 00001-00894.
We’ve drafted a message you can send Nihon Kohden to request your refund or repair — edit it as you like.
Subject: Recall Z-1162-2021 — Nihon Kohden Nihon Kohden Hello, I own a Nihon Kohden that is covered by recall Z-1162-2021 from Nihon Kohden. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
