Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Octopus 101 Perimeter Recalled by Haag-Streit USA Inc Due to The firm recalled the device after learning of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Haag-Streit USA Inc directly.
Affected Products
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.
Quantity: 64 units
Why Was This Recalled?
The firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Haag-Streit USA Inc
Haag-Streit USA Inc has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report