Collins Aerospace recalls TASE 400 Imaging systems due to a miscalculated Nominal Ocular Hazard Distance (NOHD) in Class lllb alignment lasers. This could pose a risk of eye injury during normal use. Affected units may need to be returned or repaired.
the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of imaging systems has been miscalculated.
Collins Aerospace is recalling TASE 400 Imaging systems because the safety distance for their Class lllb alignment lasers was miscalculated. This could lead to eye injuries if the laser is used without proper safety measures.
The miscalculated Nominal Ocular Hazard Distance (NOHD) means the safety distance for the laser could be too short. This increases the risk of eye injury if the laser is used without proper safety precautions.
Users of TASE 400 Imaging systems are likely affected. Those working with the equipment in environments where precise laser alignment is needed may be at higher risk.
Check for TASE 400 Imaging systems with the model name 'TASE 400'. The recall applies to all units sold by Collins Aerospace.
Identify if your TASE 400 Imaging system has the model name 'TASE 400' as listed in the recall.
The Nominal Ocular Hazard Distance (NOHD) associated with the Class lllb alignment laser was miscalculated, which could increase the risk of eye injury.
The recall does not specify an immediate stop-use requirement; however, you should check if your unit is affected and follow the provided steps.
Check for the model name 'TASE 400' on your device. The recall applies to all units sold by Collins Aerospace.
We’ve drafted a message you can send Collins Aerospace to request your refund or repair — edit it as you like.
Subject: Recall Z-1783-2019 — Collins Aerospace Collins Aerospace Hello, I own a Collins Aerospace that is covered by recall Z-1783-2019 from Collins Aerospace. 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.
