PlainRecalls

Stryker Leibinger GmbH & Co. Kg

Compiled from official public sources by the publisher.

25 recalls on record · Latest: May 29, 2024

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Agency notice ledger

Federal filing book Stryker Leibinger GmbH MID-BOOK · SINGLE-AGENCY

#662 of 14,151 · 25 notices · 0.024% archive

  • BOOK 25 notices
  • RANK #662 of 14,151
  • SHARE 0.024% archive
  • AGENCY FDA Devices (25)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 29, 2024
  • PHOTO Asp Global, LLC. dba…

Nearest notice-volume peer: Asp Global, LLC. dba Anatomy Supply Partners, LLC. (0 notice gap)

Stryker Leibinger GmbH & Co. Kg accounts for about 0.024% of the 104,423-notice archive on 25 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 →

Where Stryker Leibinger GmbH sits among 14,151 recalling firms

Stryker Leibinger GmbH & Co. Kg ranks 662nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Stryker Leibinger GmbH vs all firms by recall-notice count

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

25 662nd of 14151 higher than 13,484 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 · 2026-09-14

Stryker Leibinger GmbH in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Stryker Leibinger GmbH & Co. Kg holds about 0.024% of archive notices alongside 25 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate May 29, 2024

8000-021-002, Scopis¿ ENT Software with TGS¿ with Sofware Version: NOVA 3.6.0 RC16. Scopis is a next-generation solution for navigating functional endoscopic sinus surgery (FESS) offering surgeons highly advanced image guidance and visualization capabilities in a single system. The Stryker Electromagnetic Navigation Unit (8000-010-003) powered by Scopis ENT Software with TGS (8000-021-002), allows the analysis and identification of sinus cells in the complex patient anatomy and planning of the

FDA Devices Moderate May 15, 2024

Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the bony areas of the cranial skeleton. Catalog Number: 56-90614
FDA Devices Moderate Mar 15, 2023

Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis
FDA Devices Moderate Mar 9, 2022

MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032
FDA Devices Moderate Apr 28, 2021

DirectInject consists of a sterile dual paste system which is calcium phosphate based. Upon injection through the Mixer-Cannula, the two pastes form a cement paste which is moldable. The injected cement paste will harden under normal body conditions to form hydroxyapatite.
FDA Devices Moderate Sep 5, 2018

AXS PP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01540S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 1X20MM BURR HOLE COVER, 2 X 2- HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01526S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 1X14MM BURR HOLE COVER, 2 X 2- HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01524S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

AXS PP, 3 X 2-HOLE PLATES WITH TAB, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01541S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01521S The Stryker QuickFlap Sterile Procedure Pack is intended for reconstruction, stabilization and/or rigid fixation of non-load bearing bony areas subsequent to craniotomy, craniectomy and cranial fractures in adults and adolescents (age 12 and higher).
FDA Devices Moderate Sep 5, 2018

AXS PP, 1X14MM BURR HOLE COVER, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01548S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 3 X 2-HOLE PLATES WITH TAB, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01522S, for use on the cranium.
FDA Devices Moderate Sep 5, 2018

AXS PP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01541S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

AXS PP, 1X14MM BURR HOLE COVER, 2 X 2-HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01544S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 1X14MM BURR HOLE COVER, 2 X 2- HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01534S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 1X14MM BURR HOLE COVER, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01528S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

AXS PP, 1X20MM BURR HOLE COVER, 2 X 2-HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01546S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01531S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01520S The Stryker QuickFlap Sterile Procedure Pack is intended for reconstruction, stabilization and/or rigid fixation of non-load bearing bony areas subsequent to craniotomy, craniectomy and cranial fractures in adults and adolescents (age 12 and higher).
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 1X14MM BURR HOLE COVER, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01538S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 3 X 2-HOLE PLATES WITH TAB, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01532S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01530S, for use on the cranium
FDA Devices Moderate Sep 5, 2018

QUIKFLAP, 1X20MM BURR HOLE COVER, 2 X 2- HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01536S, for use on the cranium
FDA Devices Moderate Feb 15, 2017

9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design M Malar Sizer Set (Silicone, Non-Sterile) 9952 Extended Contoured, Malar Sizer Set (Silicone, Non-Sterile) 85000 Petite Nasal Dorsum Sizer Set (Silicone, Non-Sterile) Accessories to Medpor Implants
FDA Devices Moderate Feb 15, 2017

QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes (Sterile) Accessories to TLS Surgical Drainage System

Stryker Leibinger GmbH 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.

Asp Global, LLC. dba Anatomy Supply Partners, LLC. 25 Carefusion 25 Radiometer America Inc 25 Allergan PLC 26

Frequently Asked Questions

How many federal recall notices name Stryker Leibinger GmbH? ▼
PlainRecalls indexes 25 distinct federal recall events naming Stryker Leibinger GmbH & Co. Kg, 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 Stryker Leibinger GmbH sit among other recalling firms? ▼
Stryker Leibinger GmbH & Co. Kg ranks #662 of 14,151 by distinct recall-event count among 14,151 firms in this archive (95th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Stryker Leibinger GmbH's notices? ▼
FDA Devices accounts for 25 of this firm's 25 indexed notices.
What product category dominates Stryker Leibinger GmbH's filing book? ▼
Filings for Stryker Leibinger GmbH & Co. Kg 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.
Stryker Leibinger GmbH & Co. Kg: 25 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 Stryker Leibinger GmbH & Co. Kg; individual notices remain authoritative on each linked recall page.

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