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Model Number N/A |
Device Problem
Patient-Device Incompatibility (2682)
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Patient Problems
Hypersensitivity/Allergic reaction (1907); Unspecified Infection (1930); Skin Irritation (2076)
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Event Type
Injury
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Manufacturer Narrative
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Pma/ 510k #: p850022/s017.The warnings in the package insert state this type of event can occur.The product was discarded by the patient and therefore will not be returned for an evaluation.Because the lot number is unknown, the device history records could not be pulled and reviewed.The patient advised she has always been sensitive to adhesives.Current information is insufficient to permit a valid conclusion about the cause of this event.If additional information is obtained that adds value to the relevant content of this report and/or a conclusion can be drawn, a follow-up report will be sent.This is report one of two for the same event.Report two of two is reported on mfr #0002242816-2016-00042.
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Event Description
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The patient reported that she received the spinalpak on (b)(6) 2016 to treat her lumbar spine.The patient states of the electrodes, 63b stuck the best, however it caused a rash that became swollen and infected.The patient advised she also used the cover patches with the electrodes.The patient advised she would change her electrodes every day because she would only wear them for twelve or more hours.The patient advised she moved the electrodes around when she changed them.The patient advised she went to her doctor who gave her a sample of topical antibiotic.
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Search Alerts/Recalls
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