ASTRA recalls Lidar System for Erosion Fl: Class 1 laser product with incorrect labeling may cause safety risks in indoor flume applications. Affected units installed above water erosion flumes.
Failure to comply event due to incorrect labeling of a class 1 laser product.
ASTRA is recalling its Lidar System for Erosion Flume Application (Model L1) due to incorrect labeling of a Class 1 laser product. This could create safety risks in indoor research environments where the device is installed above water erosion flumes with limited human access.
The product has incorrect labeling for a Class 1 laser, which may not meet safety standards. This could lead to potential safety risks if the laser is not properly labeled in an indoor research environment with limited human access.
Users of the Lidar System for Erosion Flume Application (Model L1) installed above indoor water erosion flumes are affected. Researchers with limited access to the flume area are at higher risk.
Check for the Lidar System for Erosion Flume Application (Model L1) installed above indoor water erosion flumes. The product is identified by Accession No. RH19A0069.
Verify the product has correct Class 1 laser labeling as required for indoor flume applications.
The recall states the product has incorrect labeling, which may create safety risks. The official notice does not confirm if it is safe to use without correction.
The recall does not specify a remedy, so the official notice does not state what action to take.
The affected product is the Lidar System for Erosion Flume Application (Model L1) installed above indoor water erosion flumes, identified by Accession No. RH19A0069.
We’ve drafted a message you can send ASTRA to request your refund or repair — edit it as you like.
Subject: Recall Z-2100-2019 — ASTRA ASTRA Hello, I own a ASTRA that is covered by recall Z-2100-2019 from ASTRA. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
