FDA Device recall Z-1692-2015
Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A
- FDA Device
- Class II
- terminated
- Published 2015-06-10
On 2015-06-10 the FDA classified a Class II recall of Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A by Smiths Medical Asd, citing the Auxiliary Serial Input/ Output Modes on the Advisor do not function as expected, resulting in data formatting issues or incorrect data being transmitted in or out of the seria….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1692-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-21 |
| Published | 2015-06-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Smiths Medical Asd |
| Distribution | MN |
Product
Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A.
Reason
The Auxiliary Serial Input/ Output Modes on the Advisor do not function as expected, resulting in data formatting issues or incorrect data being transmitted in or out of the serial port into a data collection system.
Identifiers
| code_info | Serial Numbers: 4059587 through 4059591 UPDATED 4-20-2015: additional devices affected have serial numbers: 40599…Serial Numbers: 4059587 through 4059591 UPDATED 4-20-2015: additional devices affected have serial numbers: 4059949, 4059950, 4059951, 4059952, 4059953, 4059954, 4059955, 4059957, 4059958 and 4059960 |
|---|
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-1692-2015%22
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