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ORTHO SOLUTIONS Recalls
4 recalls on record · October 14, 2015 to March 21, 2018 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 21, 2018Medical DevicesFDA
ORTHO SOLUTIONS, LTD. recalls SYSTEM 26. Part Numbers: OS900035-NS; OS900036-NS; OS900037-NS; OS900038-NS; OS900040-NS; OS900041-NS; OS900042-N
Hazard: Following the identification of corrosion residue found inside the cannulated devices in Forefoot and Midfoot trays Orhto Solutions Group has taken the decision to recall ALL x106 System 26 Forefoot and Midfoot Implants and Instruments tray from the US market.
August 9, 2017Medical DevicesFDA
Ortho Solutions Inc recalls Oxford/Oxbridge AFN End Cap 10 mm x 5 mm tp 12 mm x10 mm The end caps are a circular disk with a small threaded sha
Hazard: There is a material mislabeling of the AFN End Cap.
September 28, 2016Medical DevicesFDA
Ortho Solutions Inc recalls FPS 35mm x 3.5 mm non-locking screw
Hazard: Mislabeling of a single batch of FPS 3.5 x 35 mm Locking Screw as being Non-Locking Screws.
October 14, 2015Medical DevicesFDA
Ortho Solutions Inc recalls Ortho OS Solutions UltOS 3.5mm locking screw 12mm to 50mm Ortho Solutions LTD, Unit 5 West Station Business Park, Spital
Hazard: Ortho Solutions Inc is initiating a recall on behalf of UltOS 3.5mm locking screw. The locking thread feature of the screw was not manufactured to specification. As a consequence there is a risk that a screw may not lock onto the plate at the time of primary insertion into the plate and the bone. In the event of this occurring the non functioning screw would need to be replaced with an alternativ