Catalog Number RONYX25026UX |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
|
Patient Problems
Hypersensitivity/Allergic reaction (1907); Reaction (2414)
|
Event Date 07/19/2018 |
Event Type
Injury
|
Manufacturer Narrative
|
If information is provided in the future, a supplemental report will be issued.
|
|
Event Description
|
It is reported that a patient had two resolute onyx drug eluting stents implanted.It was noted by the patient that that they had an allergy to cobalt.The patient is following up with the implanting physician and the dermatologist that diagnosed the allergy.
|
|
Manufacturer Narrative
|
If information is provided in the future, a supplemental report will be issued.
|
|
Manufacturer Narrative
|
If information is provided in the future, a supplemental report will be issued.
|
|
Search Alerts/Recalls
|