Stryker GmbH recalls
Every recall we track for Stryker GmbH — 75 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 3 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Stryker GmbH more than tripled in 2025 (5, up from 1 in 2024). 4% rated “stop using now”.
All FDA recall records for Stryker GmbH since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 4 | 19 | 1 | 24 |
| 2019 | 0 | 2 | 16 | 0 | 18 |
| 2020 | 3 | 1 | 12 | 0 | 16 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 2 | 3 | 0 | 5 |
| 2026 (to date) | 0 | 4 | 1 | 2 | 7 |
Most common reasons for Stryker GmbH recalls
What to do if you have a recalled Stryker GmbH product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Stryker GmbH recalls
21 shown- Use cautionMedical device
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.
Stryker recalls Hoffmann II Connecting Rod Micro 3 x 40mm (Catalog 50796040) due to potential cracking after cleaning and sterilization. Affected units may require replacement.
StrykerJul 1, 2026 - Lower riskMedical device
Stryker GmbH recalls Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System. Catalog Number: 84250320S.
Stryker recalls Gamma4 Right Long Nail (catalog 84250320S) due to being manufactured with left nail geometry. This could cause improper function in surgical procedures.
StrykerMay 28, 2025 - Lower riskMedical device
Stryker GmbH recalls Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
Stryker recalls LEFT T2 GTN 8x300 mm nails that were mislabeled as left but contained right nails and vice versa. This mix-up could lead to incorrect surgical use.
StrykerMay 22, 2025 - Use cautionMedical device
Stryker GmbH recalls Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;
Stryker recalls Guide Wire with Ruler Tube 3x800 mm DIA (catalog 2351-3080S) due to risk of metal ring detaching during surgery. Affected units have specific lot numbers.
StrykerMar 28, 2025 - Lower riskMedical device
Stryker GmbH recalls Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Stryker recalls Hoffman LRF Wire Tensioner REF 4933-9-100 due to potential wire tension misalignment from a loose adjustment ring. Affected units include Lot #J43995 with UDI-DI 07613252611035.
StrykerMay 9, 2024 - Lower riskMedical device
Stryker GmbH recalls stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400; Orthopedic external fixation device intended to keep
Stryker recalls specific models of Hoffmann LRF Bone Transport Struts due to oversized thread pitch causing improper locking. Affected units have serial numbers listed in the recall notice.
StrykerFeb 7, 2023 - Lower riskMedical device
Stryker GmbH recalls Smart Toe II Intramedullary Arthrodesis Implant
Stryker recalls Smart Toe II Intramedullary Arthrodesis Implants with potential nickel sensitivity label errors. Affected models have a label showing 'Indicated for patients with Nickel sensitivity' instead of 'Not Indicated'.
StrykerMar 28, 2022 - Lower riskMedical device
Stryker GmbH recalls Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-13 (SPI Elast. Sleeve 8-13), Catalog Number 18061407S
Stryker recalls elastic T2 Tibia SPI sleeves with incorrect inner diameter labeling. This may cause improper nail insertion. Affected units have specific catalog and lot numbers.
StrykerMay 27, 2021 - Lower riskMedical device
Stryker GmbH recalls Osteosynthesis Compression Staple EasyClip
Stryker recalls Osteosynthesis Compression Staple EasyClip products for potential nickel release in children under 20 kg when 2+ implants are used. Affected models include EasyClip and EasyClip Xpress sizes up to 25x22x22mm.
StrykerSep 25, 2020 - Stop using nowMedical device
Stryker GmbH recalls Stryker Compression Screw, Advanced T2 Tibia Catalog Number: 18220001S - Product Usage: Stryker implants are single use
Stryker recalls Advanced T2 Tibia Compression Screws (Catalog 18220001S) due to potential blister pack compromise affecting sterility. This single-use medical implant may not be sterile if the packaging is damaged.
StrykerMay 7, 2020 - Use cautionMedical device
Stryker GmbH recalls Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support
Stryker recalls T2 Alpha Delta Strike Plate instruments due to potential breakage during nail procedures, which may cause complications. Affected units include specific model and lot numbers.
StrykerDec 5, 2019 - Use cautionMedical device
Stryker GmbH recalls Stryker Pin To Rod Coupling External Fixation System Hoffmann II Compact - Pin To Rod Coupling 5/3-4mm Catalog #:
Stryker recalls a pin-to-rod coupling for fracture treatment. The device may not clamp pin and rod as intended, risking improper fixation. Affected units include specific model and lot numbers.
StrykerNov 21, 2019 - Lower riskMedical device
Stryker GmbH recalls Endotrig ETF Hook Blade, Catalog Number 1052-1 The EPF system is designed for the treatment of plantar fasciosis. The
Stryker recalls Endotrig ETF Hook Blade (Catalog 1052-1) due to potential compromised sterile bag seals. This could risk infection during surgery. Affected lots: 01406, 01475.
StrykerJul 25, 2019 - Lower riskMedical device
Stryker GmbH recalls Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1
Stryker recalls Endotrac EPF/EGR Hook/Triangle Blade Kit (Catalogue 3056-1) due to potential compromised sterile bag seals. Affected units include specific lot numbers. Consumers should contact Stryker for details.
StrykerApr 30, 2019 - Lower riskMedical device
Stryker GmbH recalls Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
Stryker recalls Basic T2 Femur Long Instrument Tray (lot K026ACE/KU97181) due to risk of using wrong instrument set during knee surgery. Affected users should verify model numbers.
StrykerJan 21, 2019 - Use cautionMedical device
Stryker GmbH recalls Hoffman LRF Hexapod Strut, Extra Short 183mm-295mm, Model Number 4935-0-040. Product Usage - The Hoffmann LRF System is
Stryker recalls Hoffman LRF Hexapod Struts with model 4935-0-040 due to potential pin displacement causing instability. Affected units sold in specific lots; contact Stryker for remedy.
StrykerAug 28, 2018 - Lower riskMedical device
Stryker GmbH recalls Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002
Stryker recalls specific Hexapod software versions due to potential erroneous axial correction plans when creating correction plans with certain settings. Affected users should contact Stryker for details.
StrykerJul 26, 2018 - Lower riskMedical device
Stryker GmbH recalls Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM
Stryker recalls specific ankle and humeral nail models due to potential sterility compromise from incomplete Tyvek lid seals. Affected items include right 10mm/200mm and 12mm/200mm ankle nails, and certain humeral nails. Contact Stryker for details.
StrykerJun 27, 2018 - Lower riskMedical device
Stryker GmbH recalls Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
Stryker recalls Farabeuf Clamp for 3.5mm Screws PRO (Catalog # 705463) due to laser etching on the wrong side of the lever arm. This could cause incorrect mode detection during use.
StrykerMay 4, 2018 - Lower riskMedical device
Stryker GmbH recalls Femoral Nail, A/R T2 Femur ¿10x320 mm, Product Number 18251032S
Stryker recalls certain Femoral Nails (A/R T2 Femur 10x320 mm) due to potential reduced strength causing premature breakage. Affected units have specific product numbers and lot codes.
StrykerApr 27, 2018 - UnratedMedical device
Stryker GmbH recalls Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb
Stryker recalls Hinge Coupling Hoffmann LRF Catalog #4933-0-800 due to wrong parts being packed in packaging. This affects pediatric and adult patients needing fracture fixation. No remedy specified in official notice.
StrykerMar 12, 2018
Stryker GmbH recall questions
How many recalls has Stryker GmbH had?
75 recalls from Stryker GmbH are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Stryker GmbH recall?
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040., dated Jul 1, 2026. Every Stryker GmbH recall is listed on this page, newest first.
Why are Stryker GmbH products recalled?
The most common reasons on record: The seal integrity of the sterile bag containing the kits may be compromised. (15).
What should I do if I have a recalled Stryker GmbH product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Stryker GmbH recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.