MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-03-31 for QUADRA ALLURE MP CRT-P PM3562 manufactured by St. Jude Medical, Inc.(crm-sunnyvale).
[185689737]
The results/method and conclusion codes along with investigation results will be provided in the final report.
Patient Sequence No: 1, Text Type: N, H10
[185689740]
Related manufacturer reference number: 2938836-2020-02337;2938836-2020-02338; 2938836-2020-02339. It was reported that patient expired. There is no known allegation from a health professional that suggests the death was related to the device. It was reported that the cause of death is unknown.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2938836-2020-02336 |
MDR Report Key | 9902837 |
Report Source | OTHER |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date Mfgr Received | 2020-03-17 |
Device Manufacturer Date | 2019-07-31 |
Date Added to Maude | 2020-03-31 |
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 | ELIZABETH BOLTZ |
Manufacturer Street | 15900 VALLEY VIEW COURT |
Manufacturer City | SYLMAR CA 91342 |
Manufacturer Country | US |
Manufacturer Postal | 91342 |
Manufacturer G1 | ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) |
Manufacturer Street | 645 ALMANOR AVENUE |
Manufacturer City | SUNNYVALE CA 94085 |
Manufacturer Country | US |
Manufacturer Postal Code | 94085 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | QUADRA ALLURE MP CRT-P |
Generic Name | IMPLANTABLE PACEMAKER PULSE GENERATOR |
Product Code | NKE |
Date Received | 2020-03-31 |
Returned To Mfg | 2020-03-17 |
Model Number | PM3562 |
Catalog Number | PM3562 |
Lot Number | A000083952 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) |
Manufacturer Address | 645 ALMANOR AVENUE SUNNYVALE CA 94085 US 94085 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death | 2020-03-31 |