MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2019-09-27 for 20/30 PRIORITY PACK 20/30 INDEFLATOR 1000184 manufactured by Abbott Vascular.
| Report Number | 2024168-2019-12153 |
| MDR Report Key | 9130160 |
| Report Source | COMPANY REPRESENTATIVE,DISTRI |
| Date Received | 2019-09-27 |
| Date of Report | 2019-10-30 |
| Date of Event | 2019-09-04 |
| Date Mfgr Received | 2019-10-22 |
| Device Manufacturer Date | 2019-01-22 |
| Date Added to Maude | 2019-09-27 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| 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 | 20/30 PRIORITY PACK 20/30 INDEFLATOR |
| Generic Name | ACCESSORIES |
| Product Code | MAV |
| Date Received | 2019-09-27 |
| Returned To Mfg | 2019-10-08 |
| Catalog Number | 1000184 |
| Lot Number | 60168570 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| 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 | 2019-09-27 |