International safety notice
Corrective action for ABL90 Flex, Radiometer
Germany / BfArM · DEU · Mar 14, 2011
Key facts
| Title | Corrective action for ABL90 Flex, Radiometer |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ABL90 Flex, Radiometer |
| Manufacturer | Corrective action for ABL90 Flex, Radiometer |
| Models | WHICHFLAGSMESSAGE1310, ABL90FLEXANALYZER, WEACKNOWLEDGERECEIPTOFTHEABL90FLEXSENSORCASSETTESFIELDSAFETYNOTICE, MESSAGE1310MAYINDICATEABIASOF, REMOVALOFSC90946008OFLOTR0031, SC90–600TESTS, ASPERTHEREFERENCEMANUALTHECORRECTIVEACTIONFORMESSAGE1310ISTOREPLACETHESC, HANDLINGOFABL90FLEXSENSORCASSETTESINCASEMESSAGE1310APPEARS, HANDLINGOFSENSORCASSETTESINCASEMESSAGE1310APPEARS, WHENMESSAGE1310APPEARS, IFTHEMESSAGE1310APPEARSFORANYOFTHEPARAMETERS, RESULTINANINCORRECTDIAGNOSISANDMALTREATMENTIFTHEDECISIONISBASEDONTHERESULTSFROMTHEABL90 and 9 more |
| Date | Mar 14, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1