FDA-Device2021-05-12Class II
Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.
Medtronic Inc.
Hazard
Incorrect size printed on the device; packaging is labeled correctly.
Sold states
US Nationwide distribution in the states of NC, CO, CA, AZ, MT, MO.
Affected count
23 devices
Manufactured in
4600 Nathan Ln N, N/A, Plymouth, MN, United States
Products
Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1532-2021Don't want to check this manually?
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