FDA Device recall Z-2100-2019
Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume…
- FDA Device
- Class II
- ongoing
- Published 2019-08-14
On 2019-08-14 the FDA classified a Class II recall of Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume… by Astra, citing failure to comply event due to incorrect labeling of a class 1 laser product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2100-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-04-25 |
| Published | 2019-08-14 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Astra |
| Distribution | US |
Product
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
Reason
Failure to comply event due to incorrect labeling of a class 1 laser product.
Identifiers
| code_info | Model: L1, identified by Accession No. RH19A0069 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2100-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.