Smiths Medical — Class II medical device recall Z-1692-2015
Terminated recall by Smiths Medical ASD, Inc., reported 2015-06-10, distributed in MN. The Auxiliary Serial Input/ Output Modes on the Advisor do not function as expected, resulting in data formatt
| Recall number | Z-1692-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smiths Medical ASD, Inc., Saint Paul, MN, United States |
| Recall initiated | 2015-03-21 |
| Classified | 2015-05-29 |
| Reported by FDA | 2015-06-10 |
| Terminated | 2015-11-20 |
| Distributed | MN |
| Serial numbers | 4059587, 4059949, 4059950, 4059951, 4059952, 4059953, 4059954, 4059955, 4059957, 4059958, 4059960 |
Product
Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1692-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.