BAXTER HEALTHCARE CORPORATION PERI-GUARD; PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE
|
Back to Search Results |
|
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
|
Patient Problem
Adhesion(s) (1695)
|
Event Type
Injury
|
Manufacturer Narrative
|
The device was not returned, and the lot number is unknown; therefore, a device analysis could not be completed.Should additional relevant information become available, a supplemental report will be submitted.
|
|
Event Description
|
It was reported from an anonymous survey result that the potential patient adverse reaction for frequency of adhesion with use of peri-guard/supple peri-guard when used as a prosthesis for pericardial closure was rated moderate.The physician reported ¿i experienced moderate adhesion¿ (no further details).At the time of this report, no further detail was provided regarding if hospitalization was required, treatment for the event or the patient¿s outcome.No additional information is available.
|
|
Search Alerts/Recalls
|
|
|