Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 40mm recall — FDA Z-2828-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Recall history in this database
Classification mix: Class II: 70.
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 90mm recall — FDA Z-2831-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm recall — FDA Z-2827-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 120mm recall — FDA Z-2832-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 150mm recall — FDA Z-2833-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall — FDA Z-2829-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 60mm recall — FDA Z-2830-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceJun 18, 2025
Stryker GmbH Femoral Nail, LEFT T2 GTN 8x300 mm recall — FDA Z-1939-2025
Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but…
Class IIFDA: OngoingStryker GmbH
Medical DeviceJun 18, 2025
Stryker GmbH Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System recall — FDA Z-1914-2025
Investigation confirmed that the GAMMA4 Right Long Nail was manufactured with the geometry of a left nail.
Class IIFDA: OngoingStryker GmbH
Medical DeviceJun 18, 2025
Stryker GmbH Femoral Nail, RIGHT T2 GTN 8x300 mm recall — FDA Z-1940-2025
Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but…
Class IIFDA: OngoingStryker GmbH
Medical DeviceApr 23, 2025
Stryker GmbH Guide Wire with Ruler Tube 3x800 mm DIA recall — FDA Z-1620-2025
The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
Class IIFDA: OngoingStryker GmbH
Medical DeviceApr 23, 2025
Stryker GmbH Guide Wire with Ruler Tube 3x1000 mm DIA recall — FDA Z-1621-2025
The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
Class IIFDA: OngoingStryker GmbH
Medical DeviceJul 3, 2024
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System recall — FDA Z-2219-2024
The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.
Class IIFDA: OngoingStryker GmbH
Medical DeviceMar 8, 2023
stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400 recall — FDA Z-1191-2023
Stryker has identified a nonconformance in specific lots of Hoffmann LRF Bone Transport Struts. Specifically, the thread pitch is oversized at the distal end of the threaded rod, and as a…
Class IIFDA: OngoingStryker GmbH
Medical DeviceMay 4, 2022
Stryker GmbH Smart Toe II Intramedullary Arthrodesis Implant recall — FDA Z-1011-2022
The nickel-sensitivity statement on the outer carton may be partially covered by a label resulting in the statement showing "Indicated for patients with Nickel sensitivity" instead of "Not…
Class IIFDA: OngoingStryker GmbH
Medical DeviceNov 25, 2020
Stryker GmbH Osteosynthesis Compression Staple EasyClip recall — FDA Z-0457-2021
The device has the potential to release nickel above the acceptable margin of safety in pediatric patients who weigh less than 20 kg (44.09 lbs) when 2 or more implants are used.
Class IIFDA: OngoingStryker GmbH
Medical DeviceJun 24, 2020
Stryker Compression Screw, Advanced T2 Tibia recall — FDA Z-2374-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x37,5 mm recall — FDA Z-2383-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Humerus ¿4x32 mm recall — FDA Z-2380-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker End Cap T2 Tibia +10 mm recall — FDA Z-2375-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker End Cap, Std, Ti Gamma3 recall — FDA Z-2387-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x40 mm recall — FDA Z-2384-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker Locking Screw, Partially Threaded T2 Tibia ¿5x55 mm recall — FDA Z-2379-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker 1 End Cap T2 Humerus ¿6mm, 5mm height recall — FDA Z-2377-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Understanding this recall history
This page summarizes recall records in which the official source identifies Stryker GmbH as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.