MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-22 for ENTERRA 37800 manufactured by Medtronic Puerto Rico Operations Co..
        [176248891]
If information is provided in the future, a supplemental report will be issued.
 Patient Sequence No: 1, Text Type: N, H10
        [176248892]
Information was received from a healthcare professional (hcp) regarding a patient with an implantable neurostimulator (ins) for the treatment of gastrointestinal/pelvic floor. It was reported that the patient was hospitalized for hypoglycemia and vomiting. No further patient complications were reported as a result of this event.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3004209178-2020-01617 | 
| MDR Report Key | 9618488 | 
| Report Source | HEALTH PROFESSIONAL | 
| Date Received | 2020-01-22 | 
| Date of Report | 2020-01-22 | 
| Date of Event | 2020-01-05 | 
| Date Mfgr Received | 2020-01-09 | 
| Device Manufacturer Date | 2018-06-23 | 
| Date Added to Maude | 2020-01-22 | 
| 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 | ENTERRA | 
| Generic Name | INTESTINAL STIMULATOR | 
| Product Code | LNQ | 
| Date Received | 2020-01-22 | 
| Model Number | 37800 | 
| Catalog Number | 37800 | 
| Device Expiration Date | 2019-12-14 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | N | 
| 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. Hospitalization | 2020-01-22 |