PlainRecalls

Spinal Elements

Compiled from official public sources by the publisher.

1 recalls on record · Latest: May 30, 2018

Agency notice ledger

Federal filing book Spinal Elements SINGLE · SINGLE-AGENCY

#12,753 of 14,182 · 1 notices · 0.001% archive

  • BOOK 1 notices
  • RANK #12,753 of 14,182
  • SHARE 0.001% archive
  • AGENCY FDA Devices (1)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 30, 2018
  • PHOTO —

Spinal Elements sits #12,753 of 14,182 (12,753rd among 14,182 firms) with 1 federal notices — about 0.001% of the 104,158-record archive. Rank counts issuance frequency, not danger or fault. FDA · CPSC · NHTSA notice stamps for this firm. Read with this firm → · Dominant category →

FDA Devices Moderate May 30, 2018

AMENDIA Omega Lumbar Interbody Fusion Device, Part Number 72-00-2-092812-11 The OmegaLIF(TM) (LIF(TM)) Expandable Lumbar Interbody Device is desig…

Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.