FDA recall record

ASTRA Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage recall — FDA Z-2100-2019

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

Class IIclassification
Z-2100-2019official record ID
Aug 14, 2019report date

Recall record at a glance

Official recordZ-2100-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmASTRA, LLC
Report dateAug 14, 2019
Recall initiation dateApr 25, 2019
Quantity1 product
LocationLouisville, CO, United States

Official product description

Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume designed for modeling water erosion in an indoor research environment with limited human access

Why the product was recalled

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

Distribution information

US Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: FDA Mandated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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