PlainRecalls

SpineNet

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Sep 4, 2013

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Agency notice ledger

Federal filing book SpineNet LIGHT-BOOK · SINGLE-AGENCY

#5,810 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,810 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 4, 2013
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

SpineNet accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

SpineNet's standing among 14,151 recalling firms

SpineNet ranks 5,810th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

SpineNet vs all firms by recall-notice count

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

2 5810th of 14151 higher than 8,037 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 · 2026-09-15

SpineNet in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows SpineNet holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Sep 4, 2013

SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M). Use to aspirate bone morrow.
FDA Devices Moderate Sep 4, 2013

SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical Cage) Product Usage: Is indicated for use in skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level

SpineNet is a small archive contributor

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

Frequently Asked Questions

How many federal recall notices name SpineNet? ▼
PlainRecalls indexes 2 distinct federal recall events naming SpineNet, 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 SpineNet sit among other recalling firms? ▼
SpineNet ranks #5,810 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of SpineNet's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates SpineNet's filing book? ▼
Filings for SpineNet 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.
SpineNet: 2 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 SpineNet; individual notices remain authoritative on each linked recall page.

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