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HomeMEDTRONIC SOFAMOR DANEK, INC. › PROGENIX™ PUTTY and PROGENIX™ PLUS

PROGENIX™ PUTTY and PROGENIX™ PLUS

MEDTRONIC SOFAMOR DANEK, INC. · Model 000505 · UDI-DI 00763000140502

MBPMQV Prescription
3
510(k) clearances
185
Adverse events (1 deaths)
41
Recalls
50
Facilities

Description

DBM 000505 PROGENIX PUTTY .5CC

Recalls

DateFirmReason
2023-09-26Medtronic Sofamor Danek USA IncSpecific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requiremen
2023-09-26Medtronic Sofamor Danek USA IncSpecific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requiremen
2023-09-26Medtronic Sofamor Danek USA IncSpecific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requiremen
2023-09-26Medtronic Sofamor Danek USA IncSpecific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requiremen
2023-09-26Medtronic Sofamor Danek USA IncSpecific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requiremen
2023-09-26Medtronic Sofamor Danek USA IncSpecific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requiremen
2023-09-26Medtronic Sofamor Danek USA IncSpecific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requiremen
2023-02-08Medtronic Sofamor Danek USA IncPotential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.
2023-02-08Medtronic Sofamor Danek USA IncPotential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.
2023-02-08Medtronic Sofamor Danek USA IncPotential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.