Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes — Class II medical device recall Z-1354-2013
Terminated recall by Progressive Medical Inc, reported 2013-05-29, distributed nationwide. Product coatings require 510K approval.
| Recall number | Z-1354-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Progressive Medical Inc, Fenton, MO, United States |
| Recall initiated | 2013-04-12 |
| Classified | 2013-05-22 |
| Reported by FDA | 2013-05-29 |
| Terminated | 2014-05-07 |
| Distributed | Nationwide (US) |
| Lot numbers | 082712-02 |
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated Blade 2.50" (6.40cm) Length, Product number P0012M Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries
Reason for recall
Product coatings require 510K approval.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1354-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.