FDA recall Z-1962-2020

W. L. Gore & Associates Inc. · Class II · device

Product

Gore DrySeal Flex Introducer Sheath, Catalog #DSF1433, 33cm 14FR, Sterile. The responsible firm on the label is W. L. Gore & Associates, Inc., Flagstaff, AZ.

Reason for recall

The devices were mislabeled with the incorrect product size resulting in 16Fr devices being labeled as 14Fr devices.

Distribution

All distribution is foreign to the following countries: Austria, Belgium, Czech Republic, Denmark, Finland, France, Germany, Greece, Ireland, Italy, Japan, Norway, Spain, Sweden, Switzerland, and the UK.

Key facts

Status
Terminated
Initiation date
2019-11-18
Report date
2020-05-20
Termination date
2020-05-13
Voluntary/Mandated
Voluntary: Firm initiated
Location
Phoenix, AZ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1962-2020