Pulsion Medical Pulsiocath PiCCO ProAQT Monitoring Kit, single-use cardiac output (CO) recall — FDA Z-1121-2015
Internal testing and investigation of the packaging revealed cracks and holes in primary packaging
Overview of recall records associated with Pulsion Medical Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Internal testing and investigation of the packaging revealed cracks and holes in primary packaging
This page summarizes recall records in which the official source identifies Pulsion Medical 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.