PlainRecalls

Stryker GmbH

Compiled from official public sources by the publisher.

75 recalls on record · Latest: Aug 5, 2026

Subscribe to new Stryker GmbH recalls (RSS)

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

notices

What this shows Stryker GmbH holds about 0.072% of archive notices alongside 75 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Mar 13, 2019

Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
FDA Devices Moderate Nov 7, 2018

Hoffman LRF Hexapod Strut, Extra Short 183mm-295mm, Model Number 4935-0-040. Product Usage - The Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of: Open and closed fractures Post-traumatic joint contracture which has resulted in loss of range of motion Fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction Pseudoarthrosis or non-union of long bones Limb lengt
FDA Devices Moderate Nov 7, 2018

Hoffman LRF Hexapod Strut, Extra Short 105mm-139mm, Model Number 4935-0-020. Product Usage - The Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of: Open and closed fractures Post-traumatic joint contracture which has resulted in loss of range of motion Fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction Pseudoarthrosis or non-union of long bones Limb lengt
FDA Devices Moderate Nov 7, 2018

Hoffman LRF Hexapod Strut, Extra Short 131mm-191mm, Model Number 4935-0-030. Product Usage - The Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of: Open and closed fractures Post-traumatic joint contracture which has resulted in loss of range of motion Fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction Pseudoarthrosis or non-union of long bones Limb lengt
FDA Devices Moderate Nov 7, 2018

Hoffman LRF Hexapod Strut, Extra Short 89mm-109mm, Model Number 4935-0-010. Product Usage - The Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of: Open and closed fractures Post-traumatic joint contracture which has resulted in loss of range of motion Fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction Pseudoarthrosis or non-union of long bones Limb length
FDA Devices Moderate Oct 3, 2018

Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002
FDA Devices Moderate Aug 29, 2018

Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM 1819-1220S T2 LONG PROXIMAL HUMERAL NAIL LEFT 240mm1832-2824S T2 LONG PROXIMAL HUMERAL NAIL LEFT 280mm 1832-2828S T2 LONG PROXIMAL HUMERAL NAIL RIGHT 260mm 1832-3826S T2 Ankle Arthrd Nail lft 1818-1115S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, A/R T2 Femur ¿10x320 mm, Product Number 18251032S
FDA Devices Moderate Jul 18, 2018

Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, A/R, R1500 T2 Femur ¿12x300 mm, Product Number 18281230S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, A/R, R1500 T2 Femur ¿12x360 mm, Product Number 18281236S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, LEFT T2 GTN ¿14x300 mm, Product Number 18501430S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, RIGHT T2 GTN ¿14x460 mm, Product Number 18511446S
FDA Devices Moderate Jul 18, 2018

Ankle Arthrodesis Nail, right T2 Ankle ¿11x300mm, Product Number 18191130S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, A/R T2 Femur ¿10x340 mm, Product Number 18251034S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, A/R T2 Femur ¿15x240 mm, Product Number 18251524S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, LEFT T2 GTN ¿10x360 mm, Product Number 18501036S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S
FDA Devices Moderate Jul 18, 2018

Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, A/R, R1500 T2 Femur ¿12x380 mm, Product Number 18281238S
FDA Devices Moderate Jul 18, 2018

Femoral Nail, A/R T2 Femur ¿12x360 mm, Product Number 18251236S
FDA Devices Moderate Jun 27, 2018

Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
FDA Devices Moderate May 2, 2018

Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, bone and soft tissue reconstruction in pediatric patients and adults.

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).

Cadillac 75 Cardinal Health 75 Pita Pal Foods LP 75 Infusion Options, Inc. 76 Washington Homeopathic Products, Inc. 76

Similar medical devices volume

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

Cardinal Health 75 Infusion Options, Inc. 76 Tosoh Bioscience Inc 74 Hobbs Medical, Inc. 73

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