Stryker GmbH
75 recalls on record · Latest: Aug 5, 2026
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Agency notice ledger
Federal filing book Stryker GmbH MID-BOOK · SINGLE-AGENCY
#240 of 14,151 · 75 notices · 0.072% archive
- BOOK 75 notices
- RANK #240 of 14,151
- SHARE 0.072% archive
- AGENCY FDA Devices (75)
- CAT medical devices
- CATS 1 category
- LATEST Aug 5, 2026
- PHOTO Cadillac
Nearest notice-volume peer: Cadillac (0 notice gap)
Stryker GmbH accounts for about 0.072% of the 104,423-notice archive on 75 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 →
Stryker GmbH's standing among 14,151 recalling firms
Stryker GmbH ranks 240th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Stryker GmbH vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
75 240th of 14151 higher than 13,911 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
Stryker GmbH in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
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Stryker GmbH
75 notices
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75 notices
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What this shows Stryker GmbH holds about 0.072% of archive notices alongside 75 distinct filings.
FDA Devices Moderate Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.
FDA Devices Moderate Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.
FDA Devices Moderate Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.
FDA Devices Moderate Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 120mm. Catalog Number: 50796120.
FDA Devices Moderate Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150.
FDA Devices Moderate Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.
FDA Devices Moderate Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060.
FDA Devices Moderate Jun 18, 2025
Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
FDA Devices Moderate Jun 18, 2025
Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System. Catalog Number: 84250320S.
FDA Devices Moderate Jun 18, 2025
Femoral Nail, RIGHT T2 GTN 8x300 mm. Catalog Number: 1851-0830S.
FDA Devices Moderate Apr 23, 2025
Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;
FDA Devices Moderate Apr 23, 2025
Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;
FDA Devices Moderate Jul 3, 2024
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
FDA Devices Moderate Mar 8, 2023
stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400; Orthopedic external fixation device intended to keep bone fragments/segments in a correct anatomical position until reliable bone consolidation is achieved
FDA Devices Moderate May 4, 2022
Smart Toe II Intramedullary Arthrodesis Implant
FDA Devices Moderate Aug 11, 2021
Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-13 (SPI Elast. Sleeve 8-13), Catalog Number 18061407S
FDA Devices Moderate Aug 11, 2021
Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-11 (SPI Elast. Sleeve 8-11), Catalog Number 18061406S
FDA Devices Moderate Nov 25, 2020
Osteosynthesis Compression Staple EasyClip
FDA Devices Moderate Jun 24, 2020
Stryker Compression Screw, Advanced T2 Tibia Catalog Number: 18220001S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x37,5 mm Catalog Number: 18965037S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Humerus ¿4x32 mm Catalog Number: 18964032S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker End Cap, Std, Ti Gamma3 Catalog Number: 30051100S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x40 mm Catalog Number: 18965040S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Partially Threaded T2 Tibia ¿5x55 mm Catalog Number: 18915055S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker 1 End Cap T2 Humerus ¿6mm, 5mm height Catalog Number: 18300005S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker End Cap T2 Humerus ¿6mm, 15mm height Catalog Number: 18300015S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x30 mm Catalog Number: 18965030S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x50 mm Catalog Number: 18965050S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x35 mm Catalog Number: 18965035S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Fully Threaded S2 05x35 mm Catalog Number: 17965035S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker End Cap, Standard T2 Humerus ¿6 mm Catalog Number: 18300003S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x45 mm Catalog Number: 18965045S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Devices Moderate Jan 15, 2020
Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of nails through the Targeting Device Catalog Number: 2351-0050
FDA Devices Moderate Jan 15, 2020
Stryker Pin To Rod Coupling External Fixation System Hoffmann II Compact - Pin To Rod Coupling 5/3-4mm Catalog #: 4940-1-020 - Product Usage: Indications Distal radius fractures (intra and extra) articular Intercarpal fracture dislocations Unstable forearm fractures Unstable elbow dislocation Multiple extremity fractures Radial osteotomies Foot and ankle fractures Paediatric fractures
FDA Devices Moderate Sep 4, 2019
Endotrig ETF Hook Blade, Catalog Number 1052-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endintrak 2 Hook Blade, Catalog Number 4058-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac EPF/EGR Triangle Blade, Catalog Number 3054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac EPF/EGR Hook Blade, Angled, Catalog Number 3055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endintrak¿ 2 Hook Blade, Angled, Catalog Number 4058A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac ECTR Push Blade, Catalog Number 2053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac ECTR Triangle Blade, Catalog Number 2054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac ECTR Hook Blade, Catalog Number 2055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac EPF/EGR Triangle Blade, Angled, Catalog Number 3054A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac ECTR Hook Blade, Angled, Catalog Number 2055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Sep 4, 2019
Endotrac ECTR Triangle Blade, Angled, Catalog Number 2054A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
FDA Devices Moderate Jun 26, 2019
Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1
FDA Devices Moderate Jun 26, 2019
Endotrac ECTR Hook/Triangle Blade Kit, Catalogue Number 2056-1
Stryker GmbH carries an outsized archive share
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 (75 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Stryker GmbH? ▼
PlainRecalls indexes 75 distinct federal recall events naming Stryker GmbH, 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 GmbH sit among other recalling firms? ▼
Stryker GmbH ranks #240 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 Stryker GmbH's notices? ▼
FDA Devices accounts for 75 of this firm's 75 indexed notices.
What product category dominates Stryker GmbH's filing book? ▼
Filings for Stryker GmbH 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 GmbH: 75 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 GmbH; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026