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 2020-03-30 for ACTIVA 37601 manufactured by Medtronic Puerto Rico Operations Co..
[185546207]
Concomitant medical products: product id: 37085-60, serial#: (b)(4), implanted: (b)(6) 2012, product type: extension. Product id: 37085-60, serial#: (b)(4), implanted: (b)(6) 2012, product type: extension. Product id: 3387s-40, lot#: v875336 implanted: (b)(6) 2012, product type: lead. Product id: 3387s-40, lot#: v939307, implanted: (b)(6) 2012, product type: lead. Product id: 3387s-40, lot#: v939307, implanted: (b)(6) 2012, product type: lead. Other relevant device(s) are: product id: 37085-60, serial/lot #: (b)(4), ubd: 03-may-2016, udi#: (b)(4) ; product id: 37085-60, serial/lot #: (b)(4), ubd: 03-may-2016, udi#: (b)(4) ; product id: 3387s-40, serial/lot #: v875336, ubd: 26-aug-2014, udi#: (b)(4) ; product id: 3387s-40, serial/lot #: v939307, ubd: 01-nov-2014, udi#: (b)(4) ; product id: 3387s-40, serial/lot #: v939307, ubd: 01-nov-2014, udi#: (b)(4). If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[185546208]
Information was received from a healthcare professional (hcp) via manufacturing representative (rep) regarding a patient who was im planted with an implantable neurostimulator (ins). It was reported that the patient's system was infected and was scheduled to remove on (b)(6) 2020. No further complications were reported/anticipated.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3004209178-2020-06370 |
| MDR Report Key | 9897781 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2020-03-30 |
| Date of Report | 2020-04-01 |
| Date Mfgr Received | 2020-03-30 |
| Device Manufacturer Date | 2016-12-01 |
| Date Added to Maude | 2020-03-30 |
| 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 WOODWARD CLARK |
| Manufacturer Street | 7000 CENTRAL AVENUE NE RCW215 |
| Manufacturer City | MINNEAPOLIS MN 55432 |
| Manufacturer Country | US |
| Manufacturer Postal | 55432 |
| Manufacturer Phone | 7635263920 |
| Manufacturer G1 | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Manufacturer Street | ROAD 31, KM. 24, HM 4 CEIBA NORTE INDUSTRIAL PARK |
| Manufacturer City | JUNCOS PR 00777 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 00777 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ACTIVA |
| Generic Name | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR |
| Product Code | MHY |
| Date Received | 2020-03-30 |
| Model Number | 37601 |
| Catalog Number | 37601 |
| Device Expiration Date | 2018-05-28 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Manufacturer Address | ROAD 31, KM. 24, HM 4 CEIBA NORTE INDUSTRIAL PARK JUNCOS PR 00777 US 00777 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2020-03-30 |