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Bryan Medical Inc recalls Aeris Balloon Dilation Catheter
Recalled July 26, 2023 · FDA recall Z-2148-2023 · Bryan Medical
Hazard
Devices were mislabeled. · FDA Class II
Units
5 units
Sold at
US Nationwide distribution in the states of GA, NY, & PA.
Description
Devices were mislabeled.
Product
Aeris Balloon Dilation Catheter
Manufacturer(s)
Bryan Medical Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →