MAUDE Adverse Event Report: AV-TEMECULA-CT XIENCE ALPINE EVEROLIMUS ELUTING CORONARY STENT SYSTEM; DRUG ELUTING CORONARY STENT SYSTEM

Catalog Number	1125225-18
Health Effect - Clinical Code	Heart Failure (2206)
Date of Event	05/11/2016
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Concomitant products: stents: 2.50 x 33 mm, 2.50 x 12 mm, 2.25 x 12 mm, 2.25 x 18 mm xience alpine.There was no reported device malfunction and the product was not returned as the stent remains in the anatomy.A review of the lot history record identified no manufacturing nonconformities issued to the reported lot that would have contributed to this event.Based on the information reviewed, there is no indication of a product quality issue with respect to the design, manufacture, or labeling of the device.Based on the case information and related record review, a conclusive cause for the reported patient effects, and the relationship to the product, if any, cannot be determined.
Event or Problem Description
It was reported that a 2.25 x 18 mm xience alpine, 2.50 x 33 mm xience alpine, 2.50 x 12 mm xience alpine, 2.25 x 12 mm xience alpine, and a 2.25 x 18 mm xience alpine stents were implanted on (b)(6) 2016.On (b)(6)2016, the patient was re-admitted with cardiovascular symptoms including heart failure.It is unknown what treatment was performed.The final patient outcome is unknown and the patient was discharged to a hospice.No additional information was provided.

• Brand Name: XIENCE ALPINE EVEROLIMUS ELUTING CORONARY STENT SYSTEM
• Common Device Name: DRUG ELUTING CORONARY STENT SYSTEM
• Manufacturer (Section D): AV-TEMECULA-CT; abbott vascular; 26531 ynez road; temecula CA 92591 4628
• MDR Report Key: 5985697
• Report Number: 2024168-2016-06512
• Device Sequence Number: 544124
• Product Code: NIQ
• UDI-Device Identifier: 08717648199080
• UDI-Public: (01)08717648199080(17)190127(10)6010861
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• PMA/510(K) Number: P110019
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Health Professional
• Remedial Action: Other
• Type of Report: Initial
• Report Date (Section B): 09/28/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 01/27/2019
• Device Catalogue Number: 1125225-18
• Device Lot Number: 6010861
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/13/2016
• Initial Report FDA Received Date: 09/28/2016
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: CONCOMITANT MEDICAL DEVICES
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Weight: 60