NAImco Inc dba Richmar Inc: Medical Device Recall in 2013 - (Recall #: Z-0817-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Foam Electrodes with Carbon construction: P/N 201-1261, Cat Nos.: 201-126, 203-678, and 400-856, 1.5&quot; x 3.5&quot; 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&quot; x 2&quot; 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&quot; 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&quot; 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&quot; x 3.5&quot; 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&quot; x 3.5&quot; Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 202-5671, Cat No. 202-567, 2&quot; x 2&quot; Electrode, Foam, All Serial Numbers distributed between 11/01/2009 and 01/31/2010. Cutaneous electrode.

Product Classification:

Class II

Date Initiated: November 30, 2009

Date Posted: February 20, 2013

Recall Number: Z-0817-2013

Event ID: 63927

Reason for Recall:

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

Status: Terminated

Product Quantity: 129400 electrodes

Code Information:

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

Distribution Pattern:

Distributed in the states of GA and TN.

Voluntary or Mandated:

Voluntary: Firm initiated