Stryker Recalls
192 recalls on record · May 18, 2016 to August 12, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x37,5 mm Catalog Number: 18965037S - Product Usage: Stryker implants a
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x35 mm Catalog Number: 18965035S - Product Usage: Stryker implants are
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x30 mm Catalog Number: 18965030S - Product Usage: Stryker implants a
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker Locking Screw, Fully Threaded T2 Humerus ¿4x32 mm Catalog Number: 18964032S - Product Usage: Stryker implants a
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker Locking Screw, Partially Threaded T2 Tibia ¿5x55 mm Catalog Number: 18915055S - Product Usage: Stryker implants
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker End Cap T2 Humerus ¿6mm, 15mm height Catalog Number: 18300015S - Product Usage: Stryker implants are single u
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker 1 End Cap T2 Humerus ¿6mm, 5mm height Catalog Number: 18300005S - Product Usage: Stryker implants are single
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker End Cap, Standard T2 Humerus ¿6 mm Catalog Number: 18300003S - Product Usage: Stryker implants are single use
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S - Product Usage: Stryker implants are single use devices in
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker Compression Screw, Advanced T2 Tibia Catalog Number: 18220001S - Product Usage: Stryker implants are single us
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
June 24, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker Locking Screw, Fully Threaded S2 05x35 mm Catalog Number: 17965035S - Product Usage: Stryker implants are singl
Hazard: Seal integrity of the blister pack may be compromised and sterility cannot be assured
May 13, 2020Medical DevicesFDA
Stryker Corporation recalls Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally only). Drape/ UDI: HH2020/20858701006326
Hazard: Sterile drapes packaged in an unsealed pouch.
May 13, 2020Medical DevicesFDA
Stryker Corporation recalls Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only sold in the US. Drape/ UDI: HH2000/10858701006329; HH900
Hazard: Sterile drapes packaged in an unsealed pouch.
March 25, 2020Medical DevicesFDA
Stryker Corporation recalls Stryker, REF: 0250070450, 5.0 mm x 45 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Sterile, CE, UDI: (01) 076
Hazard: Potential diff. in the length of the sheath tube and the sheath/probe. A diff. in length could lead to the base of the sheath/probe not being fully seated in the sheath tube which could result in the distal tip of the sheath melting. This could lead to a compromised insulation, leading to unintentional flow of electricity to the patient. The sheath/probe is packaged separately.
March 25, 2020Medical DevicesFDA
Stryker Corporation recalls Stryker, REF: 0250070460, 5.0 mm x 32 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Sterile, CE, UDI: (01) 076
Hazard: Potential diff. in the length of the sheath tube and the sheath/probe. A diff. in length could lead to the base of the sheath/probe not being fully seated in the sheath tube which could result in the distal tip of the sheath melting. This could lead to a compromised insulation, leading to unintentional flow of electricity to the patient. The sheath/probe is packaged separately.
March 11, 2020Medical DevicesFDA
Stryker Corporation recalls Stryker Connected OR Cart,120 V Ref Cat. #240-099-155, Qty 1, Rx Only, Manufactured for: Stryker, 5900 Optical Court, Sa
Hazard: There is a potential problem with firm s Connected OR Cart, 120V resulting in cart monitor not attaching flush with their monitor stow handle. The product is not manufactured to specifications and is positioned on the incorrect side that may lead to monitor falling from the monitor arm and a risk of user injury.
February 19, 2020Medical DevicesFDA
Stryker Corporation recalls Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Single, REF 3910-500-471, UDI 07613327464818, Sterile R, RX Only C
Hazard: Complaints have been received regarding difficulty in removing the driver from the screw. High driver removal forces can lead to the screw pulling out still attached to the driver. This could result in an additional anchor insertion site in the bone being used.
February 19, 2020Medical DevicesFDA
Stryker Corporation recalls Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R, RX
Hazard: Complaints have been received regarding difficulty in removing the driver from the screw. High driver removal forces can lead to the screw pulling out still attached to the driver. This could result in an additional anchor insertion site in the bone being used.
January 15, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker Pin To Rod Coupling External Fixation System Hoffmann II Compact - Pin To Rod Coupling 5/3-4mm Catalog #: 494
Hazard: Pin To Rod Coupling could not clamp the pin and rod as intended
January 15, 2020Medical DevicesFDA
Stryker GmbH recalls Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertio
Hazard: Instrument can break at the level of the thread when being exposed to high forces during nail implantation or removal which can lead to complications during nail insertion and removal.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endintrak¿ 2 Hook Blade, Angled, Catalog Number 4058A-1 The EPF system is designed for the treatment of plantar fasc
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endotrac EPF/EGR Hook Blade, Angled, Catalog Number 3055A-1 The EPF system is designed for the treatment of plantar
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endotrac EPF/EGR Triangle Blade, Angled, Catalog Number 3054A-1 The EPF system is designed for the treatment of plan
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endotrac ECTR Hook Blade, Angled, Catalog Number 2055A-1 The EPF system is designed for the treatment of plantar fas
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endotrac ECTR Triangle Blade, Angled, Catalog Number 2054A-1 The EPF system is designed for the treatment of plantar
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endintrak 2 Hook Blade, Catalog Number 4058-1 The EPF system is designed for the treatment of plantar fasciosis. The
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed for the treatment of plantar fasciosis
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endotrac EPF/EGR Triangle Blade, Catalog Number 3054-1 The EPF system is designed for the treatment of plantar fasci
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.
September 4, 2019Medical DevicesFDA
Stryker GmbH recalls Endotrac ECTR Hook Blade, Catalog Number 2055-1 The EPF system is designed for the treatment of plantar fasciosis. T
Hazard: The seal integrity of the sterile bag containing the kits may be compromised.