MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2017-09-27 for NURO 3533 manufactured by Medtronic Neuromodulation.
[87513043]
A good faith effort will be made to obtain the applicable information relevant to the report. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[87513044]
The patient reported that they had pulled muscles and were on medication that set their symptom relief back with the percutaneous tibial neuromodulation (ptnm) therapy. They indicated that they didn't have the control they had before they started taking the muscle relaxants and pain pills for their pulled muscles. The patient stated that a week following this, they found out they had a urine infection, and were placed on medication for three days. It was noted that they did not have symptoms, only lower back pain. They thought this was because the muscle spasms weren't getting better. The healthcare provider (hcp) decided to take a urine sample, and it was determined that the patient had a urine infection. This was the first that the patient had ever had. It was indicated that they were waiting to see if they still had one. They didn't think so because their urgency had been better in the last couple of weeks. There were no further complications reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
[101072091]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[101073350]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[101073351]
Additional information received from the patient indicated that they had completed 14 sessions. The patient later provided contradicting information that they went through 14 sessions, and then had two extra ones. They stated that they had started the therapy at the end of (b)(6) 2017, and it was effective and perfect. All symptoms were nearly gone. It was indicated that it was going so well the first few weeks until they hurt/pulled their back a couple months into it. They didn't have any falls or trauma, they had a bad back and "sometimes it happens. " they mentioned that the sessions didn't help starting in (b)(6) 2017. They were back to square 1, and were as bad as prior to starting the therapy. They didn't know if the therapy no longer working was due to them hurting their back, the medication they were on, or them getting a urinary infection in (b)(6)2017. It was noted that the patient was on oral medication for the infection for three days, which took care of it. The patient also reported that they never felt stimulation in their bicycle seat area, but when they would turn up the "signal" to the point where their foot would tingle, sometimes it wouldn't, and sometimes it hurt on the insertion site. There were no further complications reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3007566237-2017-04083 |
| MDR Report Key | 6897719 |
| Report Source | CONSUMER |
| Date Received | 2017-09-27 |
| Date of Report | 2017-11-16 |
| Date Mfgr Received | 2017-11-16 |
| Date Added to Maude | 2017-09-27 |
| 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 NEUROMODULATION |
| Manufacturer Street | 800 53RD AVE NE |
| Manufacturer City | MINNEAPOLIS MN 554211200 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 554211200 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | NURO |
| Generic Name | STIMULATOR,PERIPHERAL NERVE,NON-IMPLANTED,FOR PELVIC FLOOR DYSFUNCTION |
| Product Code | NAM |
| Date Received | 2017-09-27 |
| Model Number | 3533 |
| Catalog Number | 3533 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Manufacturer Address | 800 53RD AVE NE MINNEAPOLIS MN 554211200 US 554211200 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2017-09-27 |