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Recall Observatory FDA recall evidence

Device product

Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-800; UDI (01)05700693938004. Model 393-800 is available in the following configurations: ABL835, ABL830, ABL827, ABL825, ABL825, ABL820, ABL817, ABL815, ABL810, ABL805 and ABL810 BG only and ABL800Basic. The FlexQ module is optional and can be added to all models and configurations.

Z-2493-2020

May 26, 2020

Class II

Product summary

Firm
Radiometer Medical ApS
Event
Event 85700
Status
Terminated
Classification
Class II
Quantity
4,615 units
Official record key
device-enforcement:Z-2493-2020

Official wording

Reason: Potential risk of patient mix-up on analyzers due to software issues.

Code information: Software versions 6.19 and below.

Distribution pattern: US - AL, AR, AZ, BM, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV and WY. OUS - Australia, Austria, Canada, Czech Republic, China, Croatia, Denmark, France, Finland, Germany, Hungary, India, Italy, Japan, Netherlands, Norway, Poland, Russia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Turkey and United Kingdom

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential risk of patient mix-up on analyzers due to software issues.