CORRecalls & reported problems across all models

We found 2 models of COR by Medos International Sàrl in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

2 FDA recall records name at least one of these models by its device identifier, 2 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

COR 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. Feb 24, 2025Open, Classified

   Device is missing the pin in the graft loader component.

   Z-1315-2025 · Root cause: Employee error · names 2 of these models · Recall details · FDA record ↗

2. Feb 24, 2025Open, Classified

   Device is missing the pin in the graft loader component.

   Z-1314-2025 · Root cause: Employee error · names 2 of these models · Recall details · FDA record ↗

COR models

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

• COR 252109

  ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
  2 recalls0 reports
• COR 252112

  ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
  2 recalls0 reports

Other Medos International Sàrl products

• TRUESPAN ORTHOCORD6 models · 4,109 reports
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• EXPEDIUM291 models · 3,312 reports
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• EXPRESSEW6 models · 2,459 reports
• OMNISPAN ORTHOCORD3 models · 1,581 reports
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• PROWLER SELECT9 models · 1,066 reports