WELCH ALLYN, INC/MORTARA recalls

16 recalls on record · latest: September 3, 2021

Official U.S. recall history for WELCH ALLYN, INC/MORTARA, compiled from official government records.

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Welch Allyn Inc Mortara recalls ELI, Burdick and McKesson brand 280 Resting Electrocardiographs (ELI 280, MLBUR280 and BUR280), Model Numbers: ELI280-D…

September 3, 2021 · Medical device recalls Moderate risk The devices malfunction under specific operator workflows.

Welch Allyn Inc Mortara recalls Surveyor S12/S19 Bedside Patient Monitor, with AM12M Acquisition Module accessory. Impacted software version of the AM1…

March 31, 2021 · Medical device recalls Moderate risk Devices do not meet IEC 60601-2-27 requirements as labeled.

Welch Allyn Inc Mortara recalls AM12M Acquisition Module accessory. Impacted software version of the AM12M is version 1.5.1 - Product Usage: indicated…

March 31, 2021 · Medical device recalls Moderate risk Devices do not meet IEC 60601-2-27 requirements as labeled.

Welch Allyn Inc Mortara recalls ELI 280 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version…

March 31, 2021 · Medical device recalls Moderate risk Devices do not meet IEC 60601-2-27 requirements as labeled.

Welch Allyn Inc Mortara recalls ELI 380 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version…

March 31, 2021 · Medical device recalls Moderate risk Devices do not meet IEC 60601-2-27 requirements as labeled.

WELCH ALLYN, INC/MORTARA recalls ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…

November 11, 2020 · Medical device recalls Moderate risk The radio within the device can become disassociated with the wireless access p…

WELCH ALLYN, INC/MORTARA recalls X12+ and patient cable for the X12+ Telemeter with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor under the following device names: PAT CBL 10WIRE AHA…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls Replaceable lead set for the Wireless Acquisition Module (WAM), which is the ECG front-end for various Electrocardiogra…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquisition and RF transmission of…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls Q-Tel. The Q-Tel RMS system is a computer-based cardiac and pulmonary rehabilitation data acquisition and editing syste…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of real time ECG display, heart rate measurement,…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls ELI PC. The ELI PC Service automatically converts resting ECG recordings collected with WAM PC patient cables and WebUp…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls S4 and patient cable for the S4 Wireless Telemeter with the following device names: CABLE 10 WIRE LF ECG SNAP ENDS AHA…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…

WELCH ALLYN, INC/MORTARA recalls H12+ and patient cable for the H12+ Holter Recorders with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP,…

March 18, 2020 · Medical device recalls Moderate risk Impacted Welch Allyn products may not meet the Defibrillation Withstand require…