StimQ Peripheral Nerve Stimulator System — Class II medical device recall Z-2932-2020
Ongoing recall by Stimwave Technologies Inc, reported 2020-09-09, distributed nationwide. The product contains a non-functional component not referenced in product labeling.
| Recall number | Z-2932-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stimwave Technologies Inc, Pompano Beach, FL, United States |
| Recall initiated | 2020-07-15 |
| Classified | 2020-09-02 |
| Reported by FDA | 2020-09-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, BE, CH, CZ, DE, ES, GB, IL, IR, IT, NL, SK, ZA |
| Quantity | 2,197 units |
| Reason classes | labeling |
| Serial numbers | 201176-1, 201176-10, 201176-11, 201176-12, 201176-13, 201176-14, 201176-15, 201176-16, 201176-17, 201176-18, 201176-19, 201176-2, 201176-20, 201176-21, 201176-22, 201176-23, 201176-24, 201176-25, 201176-26, 201176-27, 201176-28, 201176-29, 201176-3, 201176-30, 201176-31 and 475 more |
| Model numbers | TQ4-SPR-BOUS |
Product
StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US - 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.
Reason for recall
The product contains a non-functional component not referenced in product labeling.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2932-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.