The FDA has posted 6 enforcement recalls of reprocessed general & plastic surgery laparoscope devices since 2025, none of them Class I (most serious). Most recent report: Sep 23, 2026.
Reusable access port system may crack or seperate during use.
Reusable access port system may crack or seperate during use.
Reusable access port system may crack or seperate during use.
Reusable access port system may crack or seperate during use.
Reusable access port system may crack or seperate during use.
Reusable access port system may crack or seperate during use.
Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Laparoscope, General & Plastic Surgery, Reprocessed”). Informational only — verify against the FDA before acting.