Civco Medical Instruments recalls

Civco Medical Instruments has 9 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 15 Apr 2015. The most frequent reason is sterility.

Total recalls9since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 15 Apr 2015

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 9 100%Class III 0 0%

Why civco medical instruments is recalled

Sterility889%
Foreign Material111%

Product types

Other Medical Devices778%
Imaging Equipment222%

By year

2015111%
2014333%
2012556%

All civco medical instruments recalls, newest first

9 total

Reported	Class	Recall	Company	Reason	Where
15 Apr 2015Device	CLASS II	Civco Surgi-Tip Transducer Cover Sterile cm) polyethylene recalled	Civco Medical Instruments	Sterility	6 states
3 Sep 2014Device	CLASS II	CollectEVAC, Sterile device with tubing and adaptor recalled	Civco Medical Instruments	Sterility	Nationwide
29 Jan 2014Device	CLASS II	Civco Belly Board MRI, Reusable non-sterile glass fiber recalled	Civco Medical Instruments	Foreign Material	Nationwide
29 Jan 2014Device	CLASS II	Civco Belly Board, Reusable non-sterile carbon fiber belly recalled	Civco Medical Instruments	Sterility	Nationwide
18 Jul 2012Device	CLASS II	Civco VirtuTRAX Instrument Navigator recalled	Civco Medical Instruments	Sterility	6 states
18 Jul 2012Device	CLASS II	Civco General Purpose Sensor recalled by Civco Medical Instruments	Civco Medical Instruments	Sterility	6 states
18 Jul 2012Device	CLASS II	Civco General Purpose Sensor recalled by Civco Medical Instruments	Civco Medical Instruments	Sterility	6 states
18 Jul 2012Device	CLASS II	Civco General Purpose Sensor recalled by Civco Medical Instruments	Civco Medical Instruments	Sterility	6 states
18 Jul 2012Device	CLASS II	Civco VirtuTRAX Instrument Navigator recalled	Civco Medical Instruments	Sterility	6 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.