Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software Recalled by NuVasive Inc Due to Due to an incorrect security key, customers were...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact NuVasive Inc directly.
Affected Products
NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
Quantity: 7
Why Was This Recalled?
Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery, neck dissections, thoracic surgeries, and upper and lower extremity procedures.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About NuVasive Inc
NuVasive Inc has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report