Medical Device Advisories

FDA Advisory No. 2017-322 || TERMINATION OF THE VOLUNTARY PRODUCT RECALLOF COBRA DISTAL RADIUS FIXATOR

FDA Advisory No. 2017-322

TERMINATION OF THE VOLUNTARY PRODUCT RECALLOF COBRA DISTAL RADIUS FIXATOR

The Food and Drug Administration (FDA) informs the public that Orthopaedic International Inc., the Marketing Authorization Holder (MAH), has completed the recall, removal, and destruction of Cobra Distal Radius Fixator with Lot Nos. 1601022 and 1600770 from the Philippine market.

Dissemination of the above information to all concerned is requested.

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