Medical devices, 2017
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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 Poly 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 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 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 30 mm Curved 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 Curved 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 MIS Screw 5.5 x 40mm and 5.5 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 45mm Curved 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 Curved and precontoured 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 Curved and Precontoured 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 Curved 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 Curved 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 Straight 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 Straight 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 Straight 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 Straight 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 Straight 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 Straight 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 Straight 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 250mm Straight 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 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 300mm Straight 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 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 350 Straight 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 400mm Straight 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 500mm Straight 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 Awl 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 Tapper 5.5 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 Tapper 6.5 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 Wall Check 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 Driver 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 Nut Driver 4.0 Hexa and Alignment Driver 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 Rod Holder 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 Anti Torque 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 Rod Bender 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 Compressor 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 Distractor 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 Marking Pin (Smooth) 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 Marking Pin (Round Jaw) 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 Inside Bender (L) and (R) 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 Reduction A 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 Reduction B 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 Cross Link Torque Handle 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 Dilator Handle 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 Dilator A 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 Dilator B 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 Pedicle Cut 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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