FDA recall record

Haag-Streit USA HS Hi-R NEO 900 Reference # 657 820 Serial # from 101 Product Usage: A wide recall — FDA Z-2482-2019

software error in the central control unit of the floor stand.

Class IIclassification
Z-2482-2019official record ID
Sep 11, 2019report date

Recall record at a glance

Official recordZ-2482-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHaag-Streit USA Inc.
Report dateSep 11, 2019
Recall initiation dateJul 31, 2019
Quantity0
LocationMason, OH, United States

Official product description

HS Hi-R NEO 900 Reference # 657 820 Serial # from 101 Product Usage: A wide range of surgical interventions are made possible through the modular construction and the diversity of the equipment and accessories. The operating microscope HS Hi-R NEO 900/HS Hi-R NEO 900A/HS Hi-R NEO 900A NIR and HS ALLEGRA 900/590/90 are designed for use in Ophthalmology and in other disciplines where a vertical line of viewing is required. Due to their high maneuverability, the HS ALLEGRA range of operating microscopes are qualified for further applications, in particular ENT- and reconstructive microsurgery are possible, because their line of sight can be tilted or adjusted horizontally. The HS ALLEGRA 590 is particular because of its multidisciplinary application possibilities.

Why the product was recalled

software error in the central control unit of the floor stand.

Distribution information

US in the state of OH

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Visit.

What to do next

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