Foam Electrodes with Carbon construction: P/N 201-1261 — Class II medical device recall Z-0817-2013
Terminated recall by NAImco Inc dba Richmar Inc, reported 2013-02-20, distributed in GA, TN. Electrode Socket Terminal pulling away from the electrode lead wire when the electrical stim lead wire was rem
| Recall number | Z-0817-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | NAImco Inc dba Richmar Inc, Chattanooga, TN, United States |
| Recall initiated | 2009-11-30 |
| Classified | 2013-02-14 |
| Reported by FDA | 2013-02-20 |
| Terminated | 2013-09-03 |
| Distributed | GA, TN |
| Quantity | 129,400 electrodes |
| Model numbers | 1.5, 201-126, 201-127, 201-128, 201-129, 201-130, 201-137, 202-093, 202-277, 202-278, 202-567, 203-483, 203-484, 203-565, 203-673, 203-675, 203-677, 203-678, 203-679, 203-681, 400-855, 400-856, 400-873, 400-880, 400-882 |
Product
Foam Electrodes with Carbon construction: P/N 201-1261, Cat Nos.: 201-126, 203-678, and 400-856, 1.5" x 3.5" Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1271, Cat Nos.: 201-127, 202-093, 203-483, 203-565, 203-673, and 400-873, 2" x 2" Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1281, Cat Nos.: 201-128, 202-277, 203-675, and 400-873, 2" Round Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1291, Cat Nos.: 201-129, 203-677, and 400-882, 3" Round Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1301, Cat Nos.: 201-130, 203-679, and 400-855, 1.5" x 3.5" Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1371, Cat Nos.: 201-137, 202-278, 203-484, 203-681, and 400-880, 2" x 3.5" Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 202-5671, Cat No. 202-567, 2" x 2" Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010. Cutaneous electrode.
Reason for recall
Electrode Socket Terminal pulling away from the electrode lead wire when the electrical stim lead wire was removed.
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-0817-2013. 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.