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ACCU-CHEK ® PERFORMA COMBO Adverse Event — Malfunction (MDR 3011393376-2020-01557)

ACCU-CHEK ® PERFORMA COMBO Adverse Event — Malfunction (MDR 3011393376-2020-01557) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ACCU-CHEK ® PERFORMA COMBO; Generic name: BLOOD GLUCOSE MONITORING DEVICE; Manufacturer: ROCHE DIABETES CARE, INC..

DeviceACCU-CHEK ® PERFORMA COMBO
Generic nameBLOOD GLUCOSE MONITORING DEVICE
ManufacturerROCHE DIABETES CARE, INC.
Report number3011393376-2020-01557
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceOther, Foreign, Company representation
NarrativeTHE EVENT OCCURRED OUTSIDE OF THE UNITED STATES. WHILE THIS PRODUCT IS NOT SOLD IN THE UNITED STATES, IT IS LIKE OR SIMILAR TO A PRODUCT MARKETED IN THE UNITED STATES.
SourceopenFDA MAUDE (device adverse events)

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