TASE 400 Imaging systems
FDA Recall Z-1783-2019 · Posted None
Recalling FirmCOLLINS AEROSPACE
Recall StatusOpen, Classified
Product CodeRET
Date Initiated2019-01-29
Product Quantity433 in total
Reason for Recall
the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of imaging systems has been miscalculated.
Firm Action
Collins Aerospace sent a customer notification letter to affected customers,. The letter identified the affected product problem and actions to be taken. For questions contact Customer Support Team at [email protected]
Root Cause
Radiation Control for Health and Safety Act
Distribution Pattern
US Nationwide Distribution
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.