Reported Jan 21, 2026 · Ongoing
Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090 AB9G14080090 AB9G12080090 AB9U12060090…
Medtronic 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 Inc · 4600 Nathan Ln N · Plymouth, MN · 55442-2890
Is this the product you have?
- Abre Venous Self-Expanding Stent System, Model numbers
AB9G14120090AB9G12100090AB9G14080090AB9G12080090AB9U12060090AB9U14100090AB9U14080090AB9U12080090AB9U14060090AB9G14100090AB9G12060090
- Lot codes and dates
- UDI-DI (GTIN)Serial/Lot numbers
007630005473320076300054727100763000547318007630005472640064316979622500643169796300006431697962940064316979623200643169796287007630005473250064316979630000763000547257
C112511C113253C113795C117416C117482C121084C123953C133327C133329C134478C138060C150325
- UDI-DI (GTIN)
- Amount recalled
- 442
Where it was sold
- Nationwide
Why it was recalled
Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may result in stent migration.
This product could cause temporary or reversible health problems — stop using it.
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