FDA recall record

NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and recall — FDA Z-1052-2023

Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery, neck dissections, thoracic surgeries, and…

Class IIIclassification
Z-1052-2023official record ID
Feb 15, 2023report date

Recall record at a glance

Official recordZ-1052-2023
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmNuVasive Inc.
Report dateFeb 15, 2023
Recall initiation dateJul 19, 2022
Quantity7
LocationSan Diego, CA, United States

Official product description

NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US

Why the product was 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.

Distribution information

U.S. Nationwide distribution in the states of CA, FL, NC, OH, and TX.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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