FDA Device recall Z-1783-2019
TASE 400 Imaging systems
- FDA Device
- Class II
- ongoing
- Published 2019-07-03
On 2019-07-03 the FDA classified a Class II recall of TASE 400 Imaging systems by Collins Aerospace, citing the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of imaging systems has been miscalculated.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1783-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-01-29 |
| Published | 2019-07-03 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Collins Aerospace |
| Distribution | US |
Product
TASE 400 Imaging systems
Reason
the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of imaging systems has been miscalculated.
Identifiers
| code_info | TASE 400 |
|---|
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-1783-2019%22
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