Smiths Medical recalls BCI Advisor 9200 Vital Signs Monitors with specific reorder numbers due to potential printing errors in tabular data, real-time continuous printouts, and automatic interrupt print features.
Some printing modes on the devices may not function properly (tabular data printing, real-time continuous printouts, and automatic interrupt print feature).
Smiths Medical is recalling certain BCI Advisor 9200 Vital Signs Monitors because some printing functions may not work properly. This could lead to inaccurate patient monitoring data being printed, which might affect clinical decisions.
The device may print tabular data, real-time continuous printouts, and automatic interrupt print features incorrectly. This could result in inaccurate patient monitoring information being recorded, which might impact clinical decisions if the printed data is relied upon.
Healthcare facilities using the recalled BCI Advisor 9200 monitors in hospitals or clinics are most at risk. Patients monitored by these devices could potentially receive incorrect printed data.
Check for the model number 9200 on the device. Affected units have specific reorder numbers: 920654235, 920654235, 920654335A, and 920674235A. The device is intended for use in hospitals and clinics, not home settings.
Identify the model number on the device, which should be 9200 for affected units.
Confirm the reorder number matches the listed numbers: 920654235, 920654235, 920654335A, or 920674235A.
No, the device is not intended for home use and is designed for hospital or clinical settings only.
The device may not function properly in tabular data printing, real-time continuous printouts, and automatic interrupt print features.
Check the model number (9200) and reorder number against the listed numbers: 920654235, 920654235, 920654335A, or 920674235A.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2379-2018 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-2379-2018 from Smiths Medical. 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.
