UNiD Spine Analyzer (Unknown) – Rod Planning Software Error (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286929 Two cloud-based software applications within UNiD Adaptive Spine Intelligence (ASI): the UNiD HUB and the UNiD Spine Analyzer. The UNiD HUB cloud-based software is a healthcare application to receive, transfer, display, store data needed for planning a spine surgery or for post-operative follow-up (patient information, X-ray image and recommendations for planning). The UNiD Spine Analyzer cl
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
UNiD HUB is not a medical device and thus does not have a CFN or GTIN code. UNiD Spine Analyzer Product Number SW3002 UDI-DI code: 03613720286929 No lot numbers
A medical device manufacturer is recalling UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286 due to Due to software anomalies that may impact on rod planning specifically, certain optional surgical parameters may have had errors that resulted i incor. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to software anomalies that may impact on rod planning specifically, certain optional surgical parameters may have had errors that resulted i incorrect calculations displayed on system. Impacted parameters includes the following: Roussouly Classification, Real Lumbar Lordosis and Real Thoracic Kyphosis, Barrey Ratio, and Lenke Classification.
Recommended Action
Per FDA guidance
On 12/03/2024, Medtronic sent an "Urgent Medical Device Correction" notification to physician users of the UNiD HUB informing them of a software anomalies in the UNiD" HUB that may have impacted UNiD rod planning and certain optional surgical parameters (Roussouly Classification, Real Lumbar Lordosis and Real Thoracic Kyphosis, Barrey Ratio, and Lenke Classification), and may have errors that resulting in incorrect calculations displayed in the UNiD" HUB. Medtronic is also informing users of a Software update that has removed the impacted parameters. The software update was released on 12/03/2024. Customer are informed of Patient Management Recommendations: If a UNiD rod was planned without any of these four parameters and met the surgeons planned surgical objectives, no additional actions are required. As these parameters are optional for planning, there is no record of whether the parameters were utilized for surgical planning. If you are concerned that the use of these parameters may have adversely impacted a patient s sagittal balance, it is recommended to re-evaluate the surgical plan and continue to follow the patient based on your assessment of their post operative sagittal balance. Monitor patients per routine standard of care and intervene per medical judgement. Customer are instructed to: " Review this information within this letter " Healthcare providers may continue to use the UNiD HUB as instructed in the External User Guide. " Confirm via the enclosed confirmation form that this notification has been communicated within their facility with all physician users. Send the completed Customer Confirmation Form to Medtronic viaemail at neuro.quality@medtronic.com " This notice needs to be passed on to those who need to be aware within their organization that utilizes the UNiD HUB for planning and to maintain a copy of this notice in their records.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WV, WI, WY, DC, PR
Page updated: Jan 10, 2026