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 2019-04-19 for FILTERWIRE EZ 7576 manufactured by Boston Scientific Corporation.
[142495294]
It was reported that the device could not be removed via voluntary medwatch# mw5084899. A 190cm filterwire ez was selected for use in cardiac procedure. During the procedure, a bmw guidewire was inserted, filterwire was successfully deployed and des deployed proximal to the filter wire basket. Subsequently, the bmw guidewire was removed and two additional stents were deployed. However, the retrieval sheath was unable to be fed down to the wire to capture the basket. Consequently, several strategies were attempted to remove the filter but failed. After several attempts, the filter wire could not be retrieved. The basket was jailed with an additional stent that was deployed rapidly. The procedure was completed and patient returned to icu. No further complications were reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2134265-2019-04116 |
| MDR Report Key | 8531699 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2019-04-19 |
| Date of Report | 2019-04-19 |
| Date of Event | 2019-02-21 |
| Date Mfgr Received | 2019-03-28 |
| Device Manufacturer Date | 2018-11-19 |
| Date Added to Maude | 2019-04-19 |
| 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 | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | SONALI ARANGIL |
| Manufacturer Street | TWO SCIMED PLACE |
| Manufacturer City | MAPLE GROVE MN 55311 |
| Manufacturer Country | US |
| Manufacturer Postal | 55311 |
| Manufacturer Phone | 6515827403 |
| Manufacturer G1 | BOSTON SCIENTIFIC DE COSTA RICA S.R.L. |
| Manufacturer Street | 2546 CALLE PRIMERA PROPARK, COYOL |
| Manufacturer City | ALAJUELA |
| Manufacturer Country | CS |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | FILTERWIRE EZ |
| Generic Name | TEMPORARY CORONARY SAPHENOUS VEIN BYPASS GRAFT FOR EMBOLIC PROTECTION |
| Product Code | NFA |
| Date Received | 2019-04-19 |
| Model Number | 7576 |
| Catalog Number | 7576 |
| Lot Number | 0022960424 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Manufacturer Address | TWO SCIMED PLACE MAPLE GROVE MN 55311 US 55311 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2019-04-19 |