Intramedullary Bone Saw Blade Assembly Model/Catalog Number: recall status

⚠ Recalls found. Intramedullary Bone Saw Blade Assembly Model/Catalog Number is named in 5 official recalls in our current data:

• FDA Class II recall Z-2867-2026 — Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
• FDA Class II recall Z-2868-2026 — Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
• FDA Class II recall Z-2869-2026 — Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
• And 2 more listed below.