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Welch Allyn, Inc. 901028 (REF 85NXVEC-B)Recalls & reported problems

Welch Allyn, Inc. · Welch Allyn Connex Integrated Wall System with Nellcor SpO2, Braun ThermoScan PRO 4000 Thermometry, BP Cuff and Cord Management System, Integrated MacroView Otoscope and Coaxial Ophthalmoscope, SureBP Non-invasive Blood Pressure, Pulse Rate, MAP, Programmable Alarms, BP Averaging, Adult/Pediatric/Neonate Patient Support, Four USB Ports for Accessor · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Mar 21, 2025Open, Classified

    Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

    Z-1562-2025 · Root cause: Device Design · FDA record ↗

Other MONITOR,PHYSIOLOGICAL,PATIENT(WITHOUT ARRHYTHMIA DETECTION OR ALARMS) devices

All MONITOR,PHYSIOLOGICAL,PATIENT(WITHOUT ARRHYTHMIA DETECTION OR ALARMS) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.