FDA recall Z-0699-2024

Medtronic Navigation, Inc. · Class II · device

Product

Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS

Reason for recall

Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove.

Distribution

Worldwide - US Nationwide distribution in the states of AK, AL, AZ, CA and the countries of Armenia, Australia, Austria, Belgium, Canada, China, Denmark, Finland, France, Germany, Hong Kong, Hungary, Ireland, Israel, Italy, Japan, Luxembourg, Netherlands, New Zealand, Oman, Portugal, Spain, Switzerland, United Kingdom.

Key facts

Status
Ongoing
Initiation date
2023-11-28
Report date
2024-01-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lafayette, CO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0699-2024