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Recall Observatory FDA recall evidence

Device product

Cloth electrodes with Carbon construction: P/N 201-1231, Cat Nos.: 201-123, 202-454, 203-118, 203-342, 203-454, 203-493, 203-672, 400-877, and 400-877-BJC, 2" x 2" Electrode, Cloth, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1241, Cat Nos.: 201-124, 202-455, 203-340, 203-674, and 400-872, 2" Round Electrode, Cloth, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1251, Cat Nos.: 201-138, 202-276, 202-456, 203-336, 203-680, and 400-879, 3" Round Electrode, Cloth, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1381, Cat Nos.: 201-126, 203-678, and 400-856, 2" x 3.5" Electrode, Cloth, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1501, Cat Nos.: 201-150 and 400-863, 1.25" Round Electrode, Cloth, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1521, Cat No. 400-852, 3 x 5 Electrode, Cloth, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 201-1541, Cat Nos.:201-154 and 400-865 1.5 x 2.5 Oval Electrode, Cloth, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 Cutaneous electrode.

Z-0815-2013

November 30, 2009

Class II

Product summary

Firm
NAImco Inc dba Richmar Inc
Event
Event 63927
Status
Terminated
Classification
Class II
Quantity
209860 electrodes
Official record key
device-enforcement:Z-0815-2013

Official wording

Reason: Electrode Socket Terminal pulling away from the electrode lead wire when the electrical stim lead wire was removed.

Code information: All Serial Numbers distributed between 11/01/2009 and 01/31/2010

Distribution pattern: Distributed in the states of GA and TN.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Electrode Socket Terminal pulling away from the electrode lead wire when the electrical stim lead wire was removed.

Field note

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