Medtronic Navigation, Inc.: Medical Device Recall in 2024 - (Recall #: Z-0699-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 28, 2023

Date Posted: January 17, 2024

Recall Number: Z-0699-2024

Event ID: 93611

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.

Status: Ongoing

Product Quantity: 4,224

Code Information:

UDI: 00613994247865 and 00643169105669(Japan)/ Serial Numbers: 2023041143, 2023051122, 2023051457, 2023051458, 2023060918, 2023051459, 2022030438, 2023041136, 2023041141

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated