Progressive Medical Inc: Medical Device Recall in 2013 - (Recall #: Z-1351-2013)

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:

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Blade 2.50" (6.40) Length, Product number P0012, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Product Classification:

Class II

Date Initiated: April 12, 2013

Date Posted: May 29, 2013

Recall Number: Z-1351-2013

Event ID: 64931

Reason for Recall:

Product coatings require 510K approval.

Status: Terminated

Product Quantity: 150 boxes with 12 units each.

Code Information:

Lot numbers 071212-01, 082712-01 and 111212-04

Distribution Pattern:

Nationwide Distribution including AR, AZ, CA, CO, FL, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, NE, OH, OK, OR, TN, TX, WA, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated