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Intramedullary Bone SawRecalls & reported problems across all models

Biomet Orthopedics, LLC · 7 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

5 open recalls name at least one Intramedullary Bone Saw model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls
7

We found 7 models of Intramedullary Bone Saw by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

7 FDA recall records name at least one of these models by its device identifier, 5 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Intramedullary Bone Saw recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Jul 1, 2026Open, Classified

    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.

    Z-2871-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  2. Jul 1, 2026Open, Classified

    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.

    Z-2870-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  3. Jul 1, 2026Open, Classified

    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.

    Z-2869-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  4. Jul 1, 2026Open, Classified

    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.

    Z-2868-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  5. Jul 1, 2026Open, Classified

    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.

    Z-2867-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  6. Oct 25, 2019Terminated

    Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Assembly was labeled and etched as a 14 MM but measured as a 13 MM cam

    Z-0595-2020 · Root cause: Error in labeling · Recall details · FDA record ↗

  7. Oct 25, 2019Terminated

    Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Assembly was labeled and etched as a 14 MM but measured as a 13 MM cam

    Z-0594-2020 · Root cause: Error in labeling · Recall details · FDA record ↗

Intramedullary Bone Saw models

7 models, most reported first. Each model has its own page with its reports, recalls and device details.

Other Biomet Orthopedics, LLC products

All Biomet Orthopedics, LLC devices →

Sources and updates

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