ORTOMA AB recalls Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2…

Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.

On 07/28/2025, the firm sent via email an "URGENT: MEDICAL DEVICE FIELD CORRECTION" Letter to customers informing them that the Insert Adapter OTD Straight pin may partially or completely break. This malfunction, if not identified, may result in displaying incorrect information of the reaming or cup placement by OTS Hip Guide. The values displayed on the screen may not correctly represent the actual angle and position of the tool. The magnitude of the resulting error can vary and depends on the level of the weld breakage. Customers are instructed to: 1. Discontinue use and quarantine affected units until the instructions in this letter have been read, understood and acknowledged. Complete and return the attached form via email to support@ortoma.com. 2. Adhere to the following instructions: "Visual inspection: Inspect the device prior, during, and after surgery, for damages to the weld, see section visual inspection. "In case of partial or complete weld breakage, either use a replacement adapter or revert to conventional surgery. -Refer to IFU for recalibration procedure. Recalibration would lead to a slight delay in navigated surgery, estimated less than 3 minutes. -The consequence of reverting to conventional surgery would be that the user would not have the benefits of a navigated surgery. "If product should fail, ensure that item is cleaned and sterilized according to instructions and file a formal complaint. Visual inspection Inspect all affected devices to ensure that there are no visible cracks or scratches and that the pin is fixed. (Inspect the weld at a distance of around 40 cm.) -Inspect the devices prior to, during, and after surgery, see Figure 2. -A weld passes visual inspection if the pin is not possible to move and there are no visible cracks in the weld (Figure 2-a). -A weld fails the visual inspection if it is possible to move the pin and/or if there are visible cracks or breakage. For questions contact Ortoma at support@ortoma.com

• FDA enforcement recordOfficial FDA database entry for Z-2615-2025
• FDA 510(k) clearance · K232140The device's official FDA premarket clearance record
• FDA 510(k) clearance · K250086The device's official FDA premarket clearance record
• FDA device classification · OLOOfficial FDA classification for this device type
• CFR regulation · 21 CFR 882.4560The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find ORTOMA ABSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.