MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-24 for AMPLATZER DUCT OCCLUDER 9-PDA-003 manufactured by Aga Medical Corporation.
[184842787]
An event of device deformation in the sheath and inability to deploy a 5/4 ado was reported. The results of the investigation are inconclusive since the device was not returned for analysis. The device history record was reviewed to ensure that each manufacturing and inspection operation was performed and the product met all specifications. Based on the information received, the cause of the reported incident could not be conclusively determined.
Patient Sequence No: 1, Text Type: N, H10
[184842788]
On (b)(6) 2020, an amplatzer duct occluder ii (adoii) was selected for implant first. However, the adoii did not fit well in the patient's defect, although there was no problem with the adoii itself. A 5/4mm amplatzer duct occluder (ado) was selected next, using a 180/60 5f amplatzer torqvue delivery system. However, the ado deformed and got stuck within the sheath; the ado was not able to be deployed from the delivery system. The delivery system was replaced with another one, but still the ado could not be deployed. The ado was replaced with another ado, and the procedure was completed with no consequence to the patient.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2135147-2020-00128 |
| MDR Report Key | 9872074 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2020-03-24 |
| Date of Report | 2020-03-24 |
| Date of Event | 2020-02-21 |
| Date Mfgr Received | 2020-02-25 |
| Device Manufacturer Date | 2016-10-12 |
| Date Added to Maude | 2020-03-24 |
| 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 | PAMELA YIP |
| Manufacturer Street | 5050 NATHAN LANE N |
| Manufacturer City | PLYMOUTH MN 55442 |
| Manufacturer Country | US |
| Manufacturer Postal | 55442 |
| Manufacturer Phone | 6517565400 |
| Manufacturer G1 | AGA MEDICAL CORPORATION |
| Manufacturer Street | 5050 NATHAN LANE NORTH |
| Manufacturer City | PLYMOUTH MN 55442 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 55442 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | AMPLATZER DUCT OCCLUDER |
| Generic Name | TRANSCATHETER SEPTAL OCCLUDER |
| Product Code | MLV |
| Date Received | 2020-03-24 |
| Model Number | 9-PDA-003 |
| Catalog Number | 9-PDA-003 |
| Lot Number | 5682013 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | AGA MEDICAL CORPORATION |
| Manufacturer Address | 5050 NATHAN LANE NORTH PLYMOUTH MN 55442 US 55442 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization | 2020-03-24 |