Product Safety Recalls

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Medtronic Neuromodulation Recall 91296

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

Medtronic Neuromodulation Recall 91296 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0913-2023
Event ID91296
Event DescriptionVanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900C
Product TypeDevices
DistributionWorldwide distribution.
Quantity18 units
Recall ReasonSoftware anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"
Device Classification20230118
Device Code InfoGTIN 00643169890961: Lot/Serial Numbers: NPL1000794, NPL1002295, NPL1002284, NPL1002272, NPL1001670, NPL1001615, NPL1001596, NPL1001588, NPL1001591, NPL1001592, NPL1001583, NPL1001579, NPL1001558, NPL1000777, NPL1000774, NPL1000776, NPL1000453, NPL1000429,
Center Classification Date20230106
Recall Initiation Date20221203
Recalling FirmMedtronic Neuromodulation
Initial Notification Letter
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