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Haag-Streit USA Inc recalls Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the pe

Recalled September 26, 2012 · FDA recall Z-2411-2012 · Haag-Streit USA

Hazard
The firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101. · FDA Class II
Units
64 units
Sold at
Worldwide distribution: USA (nationwide) including states of: AR, CA, CT, FL, GA, IA, IL, LA, MA, MI, MN, MS, NJ, NV, NY, OH, OR, PA, SC, SD, WA, WI, and WV; and to the countries of Jamaica, Puerto Rico, and Mexico.

Description

The firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101.

Product
Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the peripheral visual field of a patient. The device projects light on various points of a curved surface, and the patient indicates whether he or she sees the light.
Manufacturer(s)
Haag-Streit USA Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Haag-Streit USA Inc recalls Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the pe | RecallWatchUSA