Isotis Orthobiologics recalls

Isotis Orthobiologics appears in 3 official U.S. recall notices indexed by RecallRadar, most recently on 2026-08-05.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095
  FDA Device · Class II · 2026-08-05 · Isotis Orthobiologics
• OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix, OsteoSurge 100 Demineralized Bone Matrix, 10cc, REF 56300100
  FDA Device · Class II · 2025-01-22 · Isotis Orthobiologics
• OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01
  FDA Device · Class II · 2025-01-22 · Isotis Orthobiologics