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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 64931

17 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
April 12, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Progressive Medical Inc

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

17 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated Needle 2.75" (6.99cm) Length, Product number P0013M, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1348-2013
Recall number
Z-1348-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
28 boxes with 12 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 071212-02

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.

device · product 2 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Blade 6.5" (16.51cm) Length, Product number P0014, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1349-2013
Recall number
Z-1349-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
19 boxes with 12 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 071212-03

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.

device · product 3 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated L Hook 33cm Length, Product number P0020, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1350-2013
Recall number
Z-1350-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
173 boxes with 6 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot numbers 071212-05 and 081712-06

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.

device · product 4 of 17

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

Z-1351-2013
Recall number
Z-1351-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
150 boxes with 12 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

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.

device · product 5 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook 33cm Length, Product number P0100 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1352-2013
Recall number
Z-1352-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
59 boxes with 6 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot numbers 071212-06 and 082712-13

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.

device · product 6 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated L Hook 44cm Length, Product number P0020X Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1353-2013
Recall number
Z-1353-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
20 boxes with 6 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-08

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.

device · product 7 of 17

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

Z-1354-2013
Recall number
Z-1354-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
20 boxes with 12 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-02

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.

device · product 8 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -Laparoscopic Electrode PTFE Coated Curved Blade 33cm Length, Product number P0019 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1355-2013
Recall number
Z-1355-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
38 boxes with 6 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 071212-04

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.

device · product 9 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -NON-STICK CAUTERY TIP PTFE Modified Coated Blade 6.5" (16.51cm) Length, Product number P0014M Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1356-2013
Recall number
Z-1356-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
27 boxes with 12 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-04

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.

device · product 10 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Spatula 33cm Length, Product number P0018 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1357-2013
Recall number
Z-1357-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
16 boxes with 6 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-05

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.

device · product 11 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook 44cm Length, Product number P0100X Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1358-2013
Recall number
Z-1358-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
60 boxes with 6 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot numbers 071212-07 and 082712-14

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.

device · product 12 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook Split 33cm Length,Product number P0020S Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1359-2013
Recall number
Z-1359-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
20 boxes with 6 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-07

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.

device · product 13 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated J Hook 33cm Length, Product number P0021, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1360-2013
Recall number
Z-1360-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
19 boxes with 6 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-09

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.

device · product 14 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Needle 2.75" (6.99cm) Length, Product number P0013 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1361-2013
Recall number
Z-1361-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
39 boxes with 12 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-03

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.

device · product 15 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Sharp Needle 2.00" (5.08cm) Length, Product number P0118 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1362-2013
Recall number
Z-1362-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
18 boxes with 12 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-15

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.

device · product 16 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated J- Hook 44cm Length, Product number P0021X Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electrosurgeries

Z-1363-2013
Recall number
Z-1363-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
4 boxes containing 6 individually packaged pieces each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-10

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.

device · product 17 of 17

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push Button Pencil With PTFE Blade and Holster, Product number P0035H Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Rx Only Electrodes used in Electrosurgeries

Z-1364-2013
Recall number
Z-1364-2013
Initiated
April 12, 2013
Classification
Class II
Status
Terminated
Recalling firm
Progressive Medical Inc
Quantity
11 boxes with 25 units each.

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product coatings require 510K approval.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Manufacturing material removal

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product coatings require 510K approval.

Code information

Lot number 082712-12

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.

Field note

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