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PUMP MMT-522LNAL PRDGM INS CL EN ML Adverse Event — Injury (MDR 2032227-2008-00373)

PUMP MMT-522LNAL PRDGM INS CL EN ML Adverse Event — Injury (MDR 2032227-2008-00373) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PUMP MMT-522LNAL PRDGM INS CL EN ML; Generic name: INFUSION PUMP; Manufacturer: MEDTRONIC MINIMED.

DevicePUMP MMT-522LNAL PRDGM INS CL EN ML
Generic nameINFUSION PUMP
ManufacturerMEDTRONIC MINIMED
Report number2032227-2008-00373
Event typeInjury
Product problemN
Date received2008-02-21
Report sourceConsumer
NarrativeCURRENTLY, IT IS UNK WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT AS NO PRODUCT HAS BEEN RETURNED. NO CONCLUSION CAN BE DRAWN AT THIS TIME. WE, THEREFORE, CONSIDER THIS REPORT COMPLETE TO THE BEST OF OUR KNOWLEDGE.
SourceopenFDA MAUDE (device adverse events)

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