Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0817-2013 — 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&q

U.S. FDA — Device Enforcement · United States · 2009-11-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0817-2013
Date of alert
2009-11-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
NAImco Inc dba Richmar Inc
Product category
device
Product type
Devices
Reported risk: Electrode Socket Terminal pulling away from the electrode lead wire when the electrical stim lead wire was removed.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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