ClearanceBrief
Recall Z-0315-2021 ยท BSZ Gas-Machine, Anesthesia

GE Healthcare, LLC

Flow Sensor Service Part, Catalog 2089610-001-S

DateSep 17, 2020
StatusOpen, Classified
ReasonFlow sensors could have damaged tubes in the form of small punctures or cuts.
Root causeProcess control
ActionGE will issue an Urgent Medical Device Correction letter to customers with affected flow sensors. This letter will inform the customer of the issue and provide safety instructions, including to inspect all inventory of Flow Sensors. GE Healthcare will replace the Flow Sensors indicated on returned customer response forms, if applicable. In the U.S., this letter will be sent by a traceable means. The letter will be sent to the following titles within the affected accounts: Chief of Anesthesia, Director of Biomedical / Clinical Engineering, and Health Care Administrator / Risk Manager. GE Hea
Quantity4794 units
DistributionU.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, Isra
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.