Overview of recall records associated with IMPULSE DYNAMICS (USA) Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
OPTIMIZER devices may cease to deliver CCM therapy if the device incorrectly detects a charging error. This may cause patients to experience heart failure symptoms similar to before…
This page summarizes recall records in which the official source identifies IMPULSE DYNAMICS (USA) Inc. 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.
