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Progressive Medical Recalls
19 recalls on record · November 7, 2012 to May 29, 2013 · Medical Devices
Recalls by year
12
13
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push Button Pencil With PTFE Blade and Holster,
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated J- Hook 44cm
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Sharp Needle 2
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Needle 2.75" (
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated J Hook 33cm
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook S
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook 4
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Spatula 33cm
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -NON-STICK CAUTERY TIP PTFE Modified Coated Blade
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -Laparoscopic Electrode PTFE Coated Curved Blade 3
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated Blade
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated L Hook 44cm L
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook 3
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Blade 2.50" (6
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated L Hook 33cm L
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Blade 6.5" (16
Hazard: Product coatings require 510K approval.
May 29, 2013Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated Needl
Hazard: Product coatings require 510K approval.
November 21, 2012Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in
Hazard: Some of the sterile packages had broken seals.
November 7, 2012Medical DevicesFDA
Progressive Medical Inc recalls Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in
Hazard: The tip of the product could come loose or unravel.