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Leventon S. A. U Recalls

1 recall on record · September 4, 2019 to September 4, 2019 · Medical Devices

September 4, 2019Medical DevicesFDA

Leventon S. A. U. recalls DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA Provide parenteral drug infusions at a constant flow without impedi

Hazard: The product lacks 510(k) clearance, and therefore is misbranded and must be removed from the U.S. market.

Leventon S. A. U Recalls | RecallWatchUSA