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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STIMWAVE TECHNOLOGIES INC. FREEDOM NEUROSTIMULATOR; SPINAL CORD NERVE STIMULATOR

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STIMWAVE TECHNOLOGIES INC. FREEDOM NEUROSTIMULATOR; SPINAL CORD NERVE STIMULATOR Back to Search Results
Model Number PDBT-915-2K
Device Problems Overheating of Device (1437); Peeled/Delaminated (1454)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 11/08/2021
Event Type  malfunction  
Manufacturer Narrative
Although the peeling is visible, the reported issue of overheating and the cause of the peeling could not be replicated.For the report of peeling: visual inspection of unit shows unusual pattern of external corrosion, including paint peeling off.The corrosion like effect also propagated into the inside of the enclosure.Per the instructions for use for the wearable antenna assembly, the approved cleaning method is the following: clean with a damp cloth, mild household cleaners will not damage the device or labels.This has been validated by stimwave per (b)(4) -cleaning and durability of markings.Based on this test report and instructions for use, the waa has been tested to withstand mild household cleaners (such as isopropyl alcohol, bleach , soap, etc).This is the first reported complaint for peeling since commercial distribution.For the report of overheating: the pcb is in good condition, with the exception of the broken rf connector solder joint.There is no evidence of overheating on the pcb.The outside thermal temperature while charging was 29.0°c, which is below the product requirements specification of 41°c (106°f).The pa failed open which does not cause excessive current draw.The device cannot overheat because there is no current draw.The likely cause of pa failure is the broken rf connector.There is evidence of intrusion of foreign matter into the enclosure, an unidentified particulate in the vicinity of the usb connector and the rf connector.The unidentified particulate did not cause the reported issue.Although the reported issue could not be replicated, the investigation found the rf connector was damaged.Based on this information, the complaint will be closed as no problem found for the reported issues of peeling and overheating.
 
Event Description
The patient reported their wearable antenna assembly gets hot and the outside is peeling.
 
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Brand Name
FREEDOM NEUROSTIMULATOR
Type of Device
SPINAL CORD NERVE STIMULATOR
Manufacturer (Section D)
STIMWAVE TECHNOLOGIES INC.
1310 park central boulevard s.
pompano beach FL 33064
Manufacturer (Section G)
STIMWAVE TECHNOLOGIES INC.
1310 park central boulevard s.
pompano beach FL 33064
Manufacturer Contact
alicia pagliaro
1310 park central boulevard s.
pompano beach, FL 33064
MDR Report Key12963610
MDR Text Key283480110
Report Number3010676138-2021-00238
Device Sequence Number1
Product Code GZB
UDI-Device Identifier00818225020150
UDI-Public0100818225020150
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K171366
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative
Reporter Occupation Other
Type of Report Initial
Report Date 12/07/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberPDBT-915-2K
Device Lot Number00365-D
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer11/16/2021
Initial Date Manufacturer Received 11/08/2021
Initial Date FDA Received12/08/2021
Was Device Evaluated by Manufacturer? Yes
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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