Progressive Medical recalls

Progressive Medical has 19 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 29 May 2013. The most frequent reason is sterility.

Total recalls19since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 29 May 2013

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 19 100%Class III 0 0%

Why progressive medical is recalled

Sterility1789%
E. coli211%

Product types

Surgical Instruments19100%

By year

20131789%
2012211%

All progressive medical recalls, newest first

19 total

Reported	Class	Recall	Company	Reason	Where
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide
29 May 2013Device	CLASS II	Ptfe Coated Disposable Electrosurgical Electrodes recalled	Progressive Medical	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.