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FDA (Device enforcement)Recalled 2022-12-03class ii

Medtronic Neuromodulation: Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900C

Hazard

Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"

Details from the source

Reason for recall: Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303" Distribution: Worldwide distribution. Quantity: 18 units Lot/code info: GTIN 00643169890961: Lot/Serial Numbers: NPL1000794, NPL1002295, NPL1002284, NPL1002272, NPL1001670, NPL1001615, NPL1001596, NPL1001588, NPL1001591, NPL1001592, NPL1001583, NPL1001579, NPL1001558, NPL1000777, NPL1000774, NPL1000776, NPL1000453, NPL1000429,

UPC codes

00643169890961

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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