Overview of recall records associated with GE Healthcare Inc. Life Sciences, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Defective Container: vial defect was identified that could potentially impact the container closure and result in a lack of sterility assurance and/or the potential for glass particles.
This page summarizes recall records in which the official source identifies GE Healthcare Inc. Life Sciences 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.
