Reported Jan 17, 2024 · Ongoing
Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS
Medtronic Navigation, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Navigation, Inc. · 200 Medtronic Drive · Lafayette, CO · 80026
Is this the product you have?
- Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS
- Lot codes and dates
- UDI00613994247865 and 00643169105669(Japan)/
- Serial Numbers
202304114320230511222023051457202305145820230609182023051459202203043820230411362023041141
- Amount recalled
- 4,224
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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