SPS Sterilization recalls

SPS Sterilization has 15 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 19 Sep 2018. The most frequent reason is sterility.

Total recalls15since 2018

Last 12 months0reported

Class I00% of total

Ongoing0latest 19 Sep 2018

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 15 100%Class III 0 0%

Why sps sterilization is recalled

Sterility15100%

Product types

Heart & Vascular Devices15100%

By year

201815100%

All sps sterilization recalls, newest first

15 total

Reported	Class	Recall	Company	Reason	Where
19 Sep 2018Device	CLASS II	Edwards Lifesciences Femoral Venous Cannula, 20F, resterilized recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Edwards Lifesciences Aortic Perfusion Cannula, 24F, resterilized recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Edwards Lifesciences Optisite Arterial Perfusion Cannula recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Boston Scientific Wallstent RP Endoprosthesis recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Edwards Lifesciences Femoral Venous Cannula, resterilized recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Edwards Lifesciences EZ Glide Aortic Cannula, 24F, resterilized recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Boston Scientific Wallstent Endoprosthesis Tracheobronchial recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Vascular Solutions Venture Rx Catheter, 6F, resterilized recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Boston Scientific Wallstent RP Endoprosthesis recalled	SPS Sterilization	Sterility	8 states
19 Sep 2018Device	CLASS II	Boston Scientific Wallstent Endoprosthesis Tracheobronchial recalled	SPS Sterilization	Sterility	8 states

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.