PlainRecalls

NuVasive Inc

Compiled from official public sources by the publisher.

36 recalls on record · Latest: Feb 15, 2023

Subscribe to new NuVasive Inc recalls (RSS)

Agency notice ledger

Federal filing book NuVasive Inc MID-BOOK · SINGLE-AGENCY

#479 of 14,151 · 36 notices · 0.034% archive

  • BOOK 36 notices
  • RANK #479 of 14,151
  • SHARE 0.034% archive
  • AGENCY FDA Devices (36)
  • CAT medical devices
  • CATS 1 category
  • LATEST Feb 15, 2023
  • PHOTO AuroMedics Pharma LLC

Nearest notice-volume peer: AuroMedics Pharma LLC (0 notice gap)

NuVasive Inc accounts for about 0.034% of the 104,423-notice archive on 36 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How NuVasive Inc compares to 14,151 recalling firms

NuVasive Inc ranks 479th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

NuVasive Inc vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

36 479th of 14151 higher than 13,667 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

NuVasive Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows NuVasive Inc holds about 0.034% of archive notices alongside 36 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Low Feb 15, 2023

NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
FDA Devices Moderate Dec 28, 2022

X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
FDA Devices Moderate Aug 3, 2022

Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4; Simplify Disc Size 2, Ht 5/MD-5; Simplify Disc Size 2, Ht 5, 5/MD-5L; Simplify Disc Size 2, Ht 6/MD-6; Simplify Disc Size 2, Ht 6, 5/MD-6L; Simplify Disc Size 3, Ht 5/LG-5; Simplify Disc Size 3, Ht 5, 5/LG-5L; Simplify Disc Size 3, Ht 6/LG-6; Simplify Disc Size 3, Ht 6, 5/LG-6L
FDA Devices Moderate Jul 29, 2020

Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal surgery.
FDA Devices Moderate May 13, 2020

NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use spinal rod that is surgically implanted using appropriate NuVasive Reline, Reline Small Stature, and Armada fixation components (i.e. Pedicle screws, hooks and/or connectors, provided non-sterile, to be sterilized by the end user).
FDA Devices Moderate Nov 28, 2012

6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

6.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

Screw Tulip , 6.25mm Rod Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

6.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

6.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

4.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

6.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

6.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

7.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

4.5mm x 35mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

5.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
FDA Devices Moderate Nov 28, 2012

Screw Tulip , 5.5mm Rod Subsequent Codes: KWP, KWQ, MNH, MNI

NuVasive Inc holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Civco Medical Instruments Co. Inc. 36 DePuy Spine, Inc. 36 Ion Beam Applications S.a. 36 Medical Action Industries Inc 36

Frequently Asked Questions

How many federal recall notices name NuVasive Inc? ▼
PlainRecalls indexes 36 distinct federal recall events naming NuVasive Inc, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does NuVasive Inc sit among other recalling firms? ▼
NuVasive Inc ranks #479 of 14,151 by distinct recall-event count among 14,151 firms in this archive (97th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of NuVasive Inc's notices? ▼
FDA Devices accounts for 36 of this firm's 36 indexed notices.
What product category dominates NuVasive Inc's filing book? ▼
Filings for NuVasive Inc span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
NuVasive Inc: 36 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming NuVasive Inc; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026