NAImco Inc dba Richmar Inc: Medical Device Recall in 2013 - (Recall #: Z-0816-2013)

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:

Cloth electrodes with Silver-Carbon construction: P/N 202-9231, Cat No. 400-899, 2&quot; x 2&quot; Electrode, Cloth, AG, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 202-9241, Cat No. 400-895, 2&quot; Round Electrode, Cloth, AG, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 202-9381, Cat No. 400-889, 2&quot; x 3.5&quot; Electrode, Cloth AG, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 202-9501, Cat No. 202-9501, 1.25&quot; Round Electrode, Cloth AG, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 400-8991, Cat Nos.: 400-877T and 400-899T, 2&quot; x 2.25&quot; Electrode, Cloth, AG, 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-0816-2013

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: 25860 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