MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-16 for ABSORB UNK ABSORB manufactured by Abbott Vascular.
[183610454]
Patient age estimated. Date of death estimated. Date of event estimated. The unique device identifier (udi) is unknown because the part and lot. Numbers were not provided. Implant date estimated. The scaffold remains in patient. The device will not be returned for evaluation. Investigation is not yet complete. A follow-up report will be submitted with all additional relevant information. Na
Patient Sequence No: 1, Text Type: N, H10
[183610455]
It was reported that the patient underwent a coronary procedure, with implantation of an absorb bioresorbable vascular scaffold. The patient had previously underwent a coronary stenting procedure, with implantation of an unspecified bare metal stent in the right coronary artery (rca) artery, leaving untreated diseased lesion proximal to the bare metal stent. The patient underwent a second coronary procedure, on an unspecified date, and a long unspecified xience stent was implanted, covering the bare metal stent and the proximal diseased lesion. Two absorb scaffolds were implanted in the proximal and mid left anterior descending (lad) artery, in overlapping fashion. Imaging was performed and noted good results. The patient was placed on dual anti-platelet therapy (dapt) post procedure and remained on dapt for three years; however, the dapt had recently been discontinued. It was reported that the patient was found dead at home. The patient had complained of not feeling well and it was assumed that the patient experienced angina and possibly in-scaffold thrombosis. No additional information was provided.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2024168-2020-02504 |
| MDR Report Key | 9837927 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2020-03-16 |
| Date of Report | 2020-03-16 |
| Date of Event | 2020-02-01 |
| Date Mfgr Received | 2020-02-22 |
| Date Added to Maude | 2020-03-16 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. LINDSEY BELL |
| Manufacturer Street | 26531 YNEZ RD. |
| Manufacturer City | TEMECULA CA 925914628 |
| Manufacturer Country | US |
| Manufacturer Postal | 925914628 |
| Manufacturer Phone | 9519143996 |
| Manufacturer G1 | ABBOTT VASCULAR, REG # 2024168 |
| Manufacturer Street | 26531 YNEZ ROAD |
| Manufacturer City | TEMECULA CA 925914628 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 925914628 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ABSORB |
| Generic Name | BIORESORBABLE SCAFFOLD |
| Product Code | PNY |
| Date Received | 2020-03-16 |
| Catalog Number | UNK ABSORB |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ABBOTT VASCULAR |
| Manufacturer Address | 26531 YNEZ RD. TEMECULA CA 925914628 US 925914628 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Death | 2020-03-16 |