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Medtronic Inc. Recall 93558

Description: Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.

Medtronic Inc. Recall 93558 Information

StatusCompleted
Mandated?Voluntary: Firm initiated
Recall NumberZ-0623-2024
Event ID93558
Event DescriptionProtege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.
Product TypeDevices
DistributionUS Nationwide distribution in the state of MN.
Quantity1
Recall ReasonSeal defects could compromise the ability of the product packaging to maintain sterility.
Device Classification20240110
Device Code InfoLot number B644679, UDI-DI 00643169728974.
Center Classification Date20240102
Recall Initiation Date20231120
Recalling FirmMedtronic Inc.
Initial Notification Telephone
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