Tobii Assistive Technology, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0766-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii P10 Device. MyTobii P10 is a portable eye-controlled communication device featuring the Tobii Eye Control system.

Product Classification:

Class II

Date Initiated: January 14, 2013

Date Posted: February 13, 2013

Recall Number: Z-0766-2013

Event ID: 64099

Reason for Recall:

Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while recharging and produced smoke with a chemical smell.

Status: Terminated

Product Quantity: 483 units

Code Information:

Product Code 510410. All units.

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated