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IDEV Technologies Recalls

1 recall on record · June 26, 2013 to June 26, 2013 · Medical Devices

June 26, 2013Medical DevicesFDA

IDEV Technologies, Inc. recalls IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for pall

Hazard: There was an error on the outer labeling of this device. The inner label was correct.

IDEV Technologies Recalls | RecallWatchUSA