Recall Z-0317-2021— GE Healthcare, LLC
Class II · Ongoing
Class II FDA medical device recall by GE Healthcare, LLC, initiated 2020-09-17. FDA's recall record names no specific 510(k) clearance for this event. Product: Flow Sensor Service Part, Catalog 2096513-001-S. Reason: Flow sensors could have damaged tubes in the form of small punctures or cuts..
- Recalling firm
- GE Healthcare, LLC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2020-09-17
- Firm location
- Waukesha, WI, United States
Product description
Flow Sensor Service Part, Catalog 2096513-001-S
Reason for recall
Flow sensors could have damaged tubes in the form of small punctures or cuts.
Data sourced from openFDA. This site is unofficial and independent of the FDA.