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 2019-04-04 for LEAD END CAP KIT 5867-3M manufactured by Mpri.
[141009057]
Concomitant medical products: 503458 lead, implanted (b)(6) 1997. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[141009058]
It was reported that the patient's implantable pulse generator system due a suspected pocket infection. The patient was treated with antibiotics and a replacement system will be implanted upon resolution of the infection. No further patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2649622-2019-05735 |
MDR Report Key | 8485485 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-04-04 |
Date of Report | 2019-04-04 |
Date of Event | 2019-03-07 |
Date Mfgr Received | 2019-03-07 |
Device Manufacturer Date | 2017-08-02 |
Date Added to Maude | 2019-04-04 |
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 | LISA ROBERTSON |
Manufacturer Street | 8200 CORAL SEA ST NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635262723 |
Manufacturer G1 | MPRI |
Manufacturer Street | ROAD 149 KM 56.3 |
Manufacturer City | VILLALBA PR 00766 |
Manufacturer Country | US |
Manufacturer Postal Code | 00766 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LEAD END CAP KIT |
Generic Name | ADAPTOR, LEAD, PACEMAKER |
Product Code | DTD |
Date Received | 2019-04-04 |
Model Number | 5867-3M |
Catalog Number | 5867-3M |
Lot Number | VA1JJ3N |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MPRI |
Manufacturer Address | ROAD 149 KM 56.3 VILLALBA PR 00766 US 00766 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2019-04-04 |