Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS
Reported: January 17, 2024 Initiated: November 28, 2023 #Z-0699-2024
Product Description
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.
Details
- Recalling Firm
- Medtronic Navigation, Inc.
- Units Affected
- 4,224
- 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.
- Location
- Lafayette, CO
Frequently Asked Questions
What product was recalled? ▼
Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS. Recalled by Medtronic Navigation, Inc.. Units affected: 4,224.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 17, 2024. Severity: Moderate. Recall number: Z-0699-2024.
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