Class IIOngoingZ-1295-2025
Integra LifeSciences Corp. recalls AURORA Surgiscope System
Possibility for the obturator to break (separate).
Integra LifeSciences C…NJMar 12, 2025
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–5 of 5 recalls
Possibility for the obturator to break (separate).
Potential that the induction seal is not completely sealed to the device tube packaging.
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.