PlainRecalls

Synthes USA Hq, Inc.

Compiled from official public sources by the publisher.

56 recalls on record · Latest: Jan 8, 2014

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Agency notice ledger

Federal filing book Synthes USA Hq, Inc. MID-BOOK · SINGLE-AGENCY

#315 of 14,151 · 56 notices · 0.054% archive

  • BOOK 56 notices
  • RANK #315 of 14,151
  • SHARE 0.054% archive
  • AGENCY FDA Devices (56)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 8, 2014
  • PHOTO Chetak New York LLC

Nearest notice-volume peer: Chetak New York LLC (0 notice gap)

Synthes USA Hq, Inc. accounts for about 0.054% of the 104,423-notice archive on 56 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Synthes USA Hq, Inc.'s standing among 14,151 recalling firms

Synthes USA Hq, Inc. ranks 315th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Synthes USA Hq, Inc. vs all firms by recall-notice count

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

56 315th of 14151 higher than 13,835 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

Synthes USA Hq, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Synthes USA Hq, Inc. holds about 0.054% of archive notices alongside 56 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Feb 13, 2013

Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit, graduated 12mm - 26mm adjustable depth, Part Number 03.613.011. Synthes Vectra System, Synthes Vectra-One System and Synthes Vectra-T System is intended for anterior plate and screw fixation of the cervical spine (C2-C7).
FDA Devices Moderate Nov 21, 2012

Synthes External Fixation System Tube to Tube Clamp, Part Number 390.007. Intended for use to provide treatment for long bone and pelvic fractures that require external fixation. Specifically, the components can be used for: Stabilization of soft tissues and fractures; Polytrauma/multiple orthopedic trauma; Vertically stable pelvic fractures, or as treatment adjunct for vertically unstable pelvic fractures; Arthrodeses and osteotomies with soft tissue problems - failures of total joints; Neut
FDA Devices Moderate Oct 10, 2012

MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS) for percutaneous instrumentation of the thoracolumbar spine. The Synthes USS are non-cervial spinal fixation devices intended for posterior pedicle screw fixation (T1-S2/ilium), posterior hook fixation (T1-L5), or anterolateral fixation (T8-L5).
FDA Devices Critical Aug 22, 2012

Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.901.001D, and VB1025.10S. Indicated for use as a water soluble implant material and for use in the control of bleeding from bone surfaces.
FDA Devices Moderate Aug 1, 2012

4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 REF 04.019.038S Manufactured or Distributed by Synthes (USA) 1101 Synthes Avenue, Monument CO 80132 4.5MM TI Multiloc Screw Length 38MM-Sterile Ref 04.019,038S. The Multiloc Screw 4.5 is used with a Multiloc PHN for treatment of proximal humerus fractures and is intended to be inserted through the Multiloc PHN until it engages the subchondral bone below the relative distal cortex (cortex closest to the humeral head,

FDA Devices Moderate Aug 1, 2012

4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 REF 04.019.028S Manufactured or Distributed by Synthes (USA) 1101 Synthes Avenue, Monument CO 80132 4.5MM TI Multiloc Screw Length 28MM-Sterile Ref 04.019,038S. The Multiloc Screw 4.5 is used with a Multiloc PHN for treatment of proximal humerus fractures and is intended to be inserted through the Multiloc PHN until it engages the subchondral bone below the relative distal cortex (cortex closest to the humeral head,

Synthes USA Hq, Inc. carries an outsized archive share

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.

Toshiba American Medical Systems Inc 56 Avanos Medical, Inc. 57 Sedecal Sa 57 Covidien Medtronic 55

Frequently Asked Questions

How many federal recall notices name Synthes USA Hq, Inc.? ▼
PlainRecalls indexes 56 distinct federal recall events naming Synthes USA Hq, 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 Synthes USA Hq, Inc. sit among other recalling firms? ▼
Synthes USA Hq, Inc. ranks #315 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Synthes USA Hq, Inc.'s notices? ▼
FDA Devices accounts for 56 of this firm's 56 indexed notices.
What product category dominates Synthes USA Hq, Inc.'s filing book? ▼
Filings for Synthes USA Hq, 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.
Synthes USA Hq, Inc.: 56 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 Synthes USA Hq, Inc.; individual notices remain authoritative on each linked recall page.

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