Philips North America Llc recalls DigitalDiagnost C90, Model No. 712034 and 712035
Recalled Product
DigitalDiagnost C90, Model No. 712034 and 712035
Hazard / Issue
There is a software login in issue that may prevent the user from logging in.
Issued by
FDA
Affected States: AZ, GA, IN, IA, MN, NE, NH, OH, TX
Lot/Code Info: 1) UDI-DI (01)00884838090699, Model 712034, serial numbers: 10000074, 10000083, 10000163, 10000188, 10001057, 10001071, 10001072, 10001079, 10001089, 10001106, 10001133, 10001136, 10001137, 10001142, 10001146, 10001169, 10001180, 10001181, 10001186, 10001203, 10001211, 10001229, 10001234, 10001276, 19861179, 19861365, 21860026, 21860084, 21861001, 21861233, 21861386, 21861415, 21861416, 21861493, 21861528, 22860017, 22860114, 22860115, 22860448, 22860454, SN19000006, SN20861092, SN20861107, SN20861108, SN20861115, SN20861125, SN20861126, and SN20861128 2) UDI-DI (01)00884838090705, Model 712035, serial numbers: 10000034, 10000098, 10001051, 10001113, 10001130, 21860040, 22860052, SN20862021, SN20862022, and SN20862024
View official government recall
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