PlainRecalls
FDA Devices Moderate Class II Ongoing

Flow Sensor Service Part, Catalog 2096513-001-S

Reported: November 11, 2020 Initiated: September 17, 2020 #Z-0317-2021

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.

Details

Recalling Firm
GE Healthcare, LLC
Units Affected
2 units
Distribution
U.S. states where product was distributed - AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI Foreign countries impacted - Australia, Canada, Czech Republic, Estonia, France, Germany, India, Indonesia, Israel, Italy, Kuwait, Latvia, Macedonia, Madagascar, Malaysia, Nicaragua, Panama, Qatar, Russia, Singapore, Slovenia, Spain, Thailand, Ukraine, United Kingdom
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
Flow Sensor Service Part, Catalog 2096513-001-S. Recalled by GE Healthcare, LLC. Units affected: 2 units.
Why was this product recalled?
Flow sensors could have damaged tubes in the form of small punctures or cuts.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 11, 2020. Severity: Moderate. Recall number: Z-0317-2021.