Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A.
Reported: June 10, 2015 Initiated: March 21, 2015 #Z-1692-2015
Product Description
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.
Details
- Recalling Firm
- Smiths Medical ASD, Inc.
- Units Affected
- 5 UPDATE 4-20-2015 to include 10 additional devices
- Distribution
- MN
- Location
- Saint Paul, MN
Frequently Asked Questions
What product was recalled? ▼
Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A.. Recalled by Smiths Medical ASD, Inc.. Units affected: 5 UPDATE 4-20-2015 to include 10 additional devices.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 10, 2015. Severity: Moderate. Recall number: Z-1692-2015.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11