FDA recall record

Stimwave Technologies StimQ Peripheral Nerve Stimulator System (PNS) Models: 1 recall — FDA Z-2930-2020

The product contains a non-functional component not referenced in product labeling.

Class IIclassification
Z-2930-2020official record ID
Sep 9, 2020report date

Recall record at a glance

Official recordZ-2930-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmStimwave Technologies Inc.
Report dateSep 9, 2020
Recall initiation dateJul 15, 2020
Quantity1424 units
LocationPompano Beach, FL, United States

Official product description

StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-TRL-BO US and 2. FR4A-TR-BO - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an electrical energy field that acts on peripheral nerves in the limbs and torso to alter the transmission of pain signals to the brain.

Why the product was recalled

The product contains a non-functional component not referenced in product labeling.

Distribution information

Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KY, KS, LA, MD, MO, MI, MN, MA, MS, NC, NM, ND, NV, NY, NE, NJ, OK, OH, OR, PR, PA, RI, SC, TN, TX, UT, VA, WA, WI and the countries of The Netherlands, Belgium, Slovakia, Switzerland, Germany, United Kingdom, Argentina, Italy, Spain, South Africa, Iran, Israel, and Czech Republic.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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