Integra LifeSciences Corp. recalls AURORA Surgiscope System. Sterile, single use device that contains a Sheath, Obturator, and Imager.

Recalled July 17, 2024 · FDA recall Z-2331-2024 · Integra LifeSciences

Hazard

Potential sheath damage that could lead to tissue damage and/or track hemorrhage. · FDA Class II

Units

14 units

Sold at

Domestic: NY, OH, & DC.

Description

Potential sheath damage that could lead to tissue damage and/or track hemorrhage.

Product

AURORA Surgiscope System. Sterile, single use device that contains a Sheath, Obturator, and Imager.

Manufacturer(s)

Integra LifeSciences Corp.

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