Medical devices, 2017
Shortlist up to four to read them side by side.
2,615 medical device recalls FDA’s Enforcement Report published in 2017, newest first; 40,450 in all since 2012.
FDA’s medical device recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 5, 2026.
2,615of 2,615 medical device recallsshown with your filters
The list
- Medical device recall PALLAS M/MAXIMIS 50mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 60mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 70mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 80mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 40mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 35mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 45mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 50mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 55mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 60mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 120mm MIS Rod Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Set Screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 5.5 x 30mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 5.5 x 50mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 6.5 x 40mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 6.5 x 45mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 6.5 x 50mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 6.5 x 55mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 7.5 x 40mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 7.5 x 45mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 7.5 x 50mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 7.5 x 55mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 5.5 x 30mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 5.5 x 35mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Polyaxial Screw and MIS Screw, 5.5 x 40mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Polyaxial and MIS Screw, 5.5 x 45mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 5.5 x 50mm and 5.5 x 5.0 mm screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 35mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 40mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 45mm and 6.5 x 4.5 screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 50mm and 6.5 x 5.0 mm screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 55mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 7.5 x 35mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 7.5 x 40mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 7.5 x 45mm screw and 7.5 x 4.5 mm screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS 7.5 x 50mm screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 7.5 x 55mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 5.5 x 45mm & 5.5 x 4.0mm, and 7.5 x 45mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 5.5 x 50mm and 5.5 x 5.0 mm screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw5.5 x 55mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 35mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 40mm and 6.5 x 4.0 mm screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 45mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 50mm and 6.5 x 5.0 mm screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS MIS Screw 6.5 x 55mm and 6.5 x 5.5 mm screw Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 5.5 x 35mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 5.5 x 40mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
- Medical device recall PALLAS M/MAXIMIS Poly Screw 5.5 x 55mm Devices are not consistent with Quality System Requirements. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide, and California and Virginia named
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Device recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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