PlainRecalls
FDA Devices Moderate Class II Terminated

CIVCO Sales Demo Kit, REF DEMOGPGUIDE, for use by CIVCO and customer sales representatives.

Reported: December 19, 2018 Initiated: November 2, 2018 #Z-0576-2019

Product Description

CIVCO Sales Demo Kit, REF DEMOGPGUIDE, for use by CIVCO and customer sales representatives.

Details

Units Affected
135 boxes
Distribution
Foreign distribution was made to Canada, Argentina, Australia, Austria, Belgium, Brazil, Chile, China, Colombia, Croatia, Cyprus, Denmark, Estonia, France, Germany, Hong Kong, India, Israel, Italy, Japan, Latvia, Lebanon, Lithuania, Netherlands, New Zealand, Philippines, Poland, Portugal, Qatar, Romania, Saudi Arabia, Singapore, South Africa, Spain, Switzerland, Taiwan, Trinidad/Tobago, Turkey, Ukraine, United Arab Emirates, and the United Kingdom.
Location
Coralville, IA

Frequently Asked Questions

What product was recalled?
CIVCO Sales Demo Kit, REF DEMOGPGUIDE, for use by CIVCO and customer sales representatives.. Recalled by CIVCO Medical Instruments Co., Inc.. Units affected: 135 boxes.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 19, 2018. Severity: Moderate. Recall number: Z-0576-2019.