The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-1784-2019·Announced 2019-07-03

Collins Aerospace TASE 500 Imaging Systems Recalled for Laser Safety Error

Collins Aerospace is recalling TASE 500 Imaging systems because the Nominal Ocular Hazard Distance for the alignment laser was miscalculated.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a miscalculation of the Nominal Ocular Hazard Distance for a Class IIIB laser, which poses a risk of eye injury. Per the rubric, risk-of-harm products where injury has not yet been reported are classified as High (Score 3).

Plain-English summary

Collins Aerospace is recalling 433 TASE 500 Imaging systems distributed nationwide in the United States. The recall is due to a miscalculation of the Nominal Ocular Hazard Distance (NOHD) associated with the Class IIIB alignment laser utilized in the TASE family of imaging systems.

The miscalculation of the NOHD means the stated safe distance for the laser may be incorrect, potentially exposing users to eye hazards. The source text does not specify the exact nature of the miscalculation or whether any injuries have occurred.

Users of these systems should contact Collins Aerospace for instructions on how to address the issue. The recall number is Z-1784-2019.

The recalled product

Product
TASE 500 Imaging systems
Manufacturer
COLLINS AEROSPACE
Affected units
433

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • TASE 500

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by COLLINS AEROSPACE under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Same manufacturer · COLLINS AEROSPACE

See all →

Similar recalls