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ASTRA Recalls

1 recall on record · August 14, 2019 to August 14, 2019 · Medical Devices

August 14, 2019Medical DevicesFDA

ASTRA, LLC recalls Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed abov

Hazard: Failure to comply event due to incorrect labeling of a class 1 laser product.

ASTRA Recalls | RecallWatchUSA