Medical DeviceOct 13, 2021
Welch Allyn Inc Mortara ELI, Burdick and McKesson brand 280 Resting Electrocardiographs recall — FDA Z-0011-2022
The devices malfunction under specific operator workflows.
Class IIFDA: OngoingWelch Allyn Inc Mortara
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Welch Allyn Inc Mortara as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.