medical Class II Updated 2023-07-26

Bryan Medical Inc recalls Aeris Balloon Dilation Catheter

Recalled Product

Aeris Balloon Dilation Catheter

Hazard / Issue

Devices were mislabeled.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model No: KG0930; UDI: +B472KG09301; Lot No. 1402309E.
View official government recall

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