Device Problems
Device Expiration Issue (1216); Device Markings/Labelling Problem (2911)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Type
malfunction
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Manufacturer Narrative
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A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
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Event Description
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It was reported that a physician is concerned with medtronic coronary stents which they have highlighted as expired or fake.
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Manufacturer Narrative
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Additional information: the physician has now confirmed that they have not seen any expired stent and that there is no medtronic product associated with this event.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
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Search Alerts/Recalls
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