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Welch Allyn Recalls

5 recalls on record · November 4, 2015 to September 22, 2021 · Medical Devices

Recalls by year

15
17
21

Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

September 22, 2021Medical DevicesFDA
Welch Allyn Inc recalls Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent measurement of human body temperature for patie
Hazard: If the device is exposed to fluid ingress and is used before the cleaning fluid has completely dried, there is a risk of the device overheating potentially causing a burn to the user or the ear canal of the patient
June 2, 2021Medical DevicesFDA
Welch Allyn Inc recalls ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount models) Model: 34XFHT-B Intended: P
Hazard: Potential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock
June 2, 2021Medical DevicesFDA
Welch Allyn Inc recalls GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Transformer is intended for use in ambulato
Hazard: Potential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock
April 19, 2017Medical DevicesFDA
Welch Allyn Inc recalls Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY, Made in China --- Distributed by Welch
Hazard: A defective electrical component in the battery charging circuit in two lots of the ProBP 2400 may potentially cause an over-voltage battery charging condition when the device is connected to the external power supply/battery charger. This potential defect resides with the device, not the battery. The over-voltage condition can result in high NiMH battery temperatures that, in some cases, can reach levels sufficient to cause melting of the plastic battery door and other adjacent plastic and foam device components.
November 4, 2015Medical DevicesFDA
Welch Allyn Inc recalls Welch Allyn KleenSpec Corded Illumination System, Vaginal Speculum Lighting System, Model Number 78x Series Illuminator,
Hazard: The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the potential to be incorrectly connected to a commonly available AC power cord instead of the illuminator low voltage transformer power cord which is supplied with the illuminator. This may result in a shattered lamp bulb and a potential electric shock hazard.
Welch Allyn Recalls | RecallWatchUSA