PlainRecalls

Zimmer Biomet Spine Inc.

Compiled from official public sources by the publisher.

8 recalls on record · Latest: Jan 10, 2024

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Agency notice ledger

Federal filing book Zimmer Biomet Spine Inc. LIGHT-BOOK · SINGLE-AGENCY

#1,855 of 14,151 · 8 notices · 0.008% archive

  • BOOK 8 notices
  • RANK #1,855 of 14,151
  • SHARE 0.008% archive
  • AGENCY FDA Devices (8)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 10, 2024
  • PHOTO Ab Sciex

Nearest notice-volume peer: Ab Sciex (0 notice gap)

Zimmer Biomet Spine Inc. accounts for about 0.008% of the 104,423-notice archive on 8 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 Zimmer Biomet Spine Inc. compares to 14,151 recalling firms

Zimmer Biomet Spine Inc. ranks 1,855th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Zimmer Biomet Spine Inc. vs all firms by recall-notice count

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

8 1855th of 14151 higher than 12,296 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

Zimmer Biomet Spine Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Zimmer Biomet Spine Inc. holds about 0.008% of archive notices alongside 8 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jan 10, 2024

Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System
FDA Devices Moderate Mar 6, 2019

Vitality¿ Spinal Fixation System.Spinal Intervertebral Body, Appliance, Fixation (non-sterile). Pedicle screw fixation is indicated for skeletally mature patients and for adolescent patients. For use in Orthopedic medical specialty area. Product Usage: The Vitality Shear-off Set Screw is not threading properly with the mating tulip head of the Vitality screws, hooks and connectors due to a manufacturing issue. These devices are indicated as an adjunct to fusion for various indications
FDA Devices Moderate Mar 6, 2019

Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is indicated for skeletally mature patients and for adolescent patients. For use in Orthopedic medical specialty area. Product Usage: The Vitality Shear-off Set Screw is not threading properly with the mating tulip head of the Vitality screws, hooks and connectors due to a manufacturing issue. These devices are indicated as an adjunct to fusion for various indications
FDA Devices Moderate Mar 6, 2019

Vitality¿ Spinal Fixation System. Spinal Interlaminal, Appliance, Fixation, (non-sterile). Pedicle screw fixation is indicated for skeletally mature patients and for adolescent patients. For use in Orthopedic medical specialty area. Product Usage: The Vitality Shear-off Set Screw is not threading properly with the mating tulip head of the Vitality screws, hooks and connectors due to a manufacturing issue. These devices are indicated as an adjunct to fusion for various indications.
FDA Devices Moderate Jun 14, 2017

Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting Handle  90 in-lbs Model Number(s): 07.02066.001, 07.02053.001, 730M0017
FDA Devices Moderate Apr 5, 2017

Altius M-INI OCT Posterior Spinal Fixation System, Model Number 1200-9216 The AltiusTM OCT and AltiusTM M-INITM OCT Systems when intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (Occiput-T3), these systems are indicated for: DDD (neck pain of discogenic origin with degeneration of the disc as confirmed by patient history and radiographic studies); spondylolisthesis; spinal stenosis; fracture/dislocation; atlantoaxial fracture with instability; occipitocervi
FDA Devices Moderate Aug 17, 2016

Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled sterile.
FDA Devices Moderate Aug 17, 2016

Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled sterile.

Zimmer Biomet Spine Inc. holds a measurable archive slice

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (8 here).

Ab Sciex 8 Acumedia Manufacturers, Inc. 8 Adept Medical Ltd 8 Aju Pharm Co., Ltd. 8 Ambriola Co., Inc., The 8

Similar medical devices volume

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

Ab Sciex 8 Acumedia Manufacturers, Inc. 8 Adept Medical Ltd 8 Aju Pharm Co., Ltd. 8

Frequently Asked Questions

How many federal recall notices name Zimmer Biomet Spine Inc.? ▼
PlainRecalls indexes 8 distinct federal recall events naming Zimmer Biomet Spine 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 Zimmer Biomet Spine Inc. sit among other recalling firms? ▼
Zimmer Biomet Spine Inc. ranks #1,855 of 14,151 by distinct recall-event count among 14,151 firms in this archive (87th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Zimmer Biomet Spine Inc.'s notices? ▼
FDA Devices accounts for 8 of this firm's 8 indexed notices.
What product category dominates Zimmer Biomet Spine Inc.'s filing book? ▼
Filings for Zimmer Biomet Spine 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.
Zimmer Biomet Spine Inc.: 8 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 Zimmer Biomet Spine Inc.; individual notices remain authoritative on each linked recall page.

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