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Urologix Recalls

1 recall on record · November 20, 2013 to November 20, 2013 · Medical Devices

November 20, 2013Medical DevicesFDA

Urologix, Inc. recalls Prostiva RF Therapy Hand Piece Kit, REF 8929, Rx only, sterilized using Ethylene Oxide. The Prostiva RF Model 8929 Ha

Hazard: A Hand Piece high deployment force exceeded the maximum specification.

Urologix Recalls | RecallWatchUSA