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Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation Recalls

All product recalls associated with Stryker Instruments Div. of Stryker Corporation.

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Recall Summary

Total Recalls

264

Past Year

Class I (Serious)

Most Recent

Oct 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 81–100 of 264 recalls

Stryker Instruments Div. of Stryker Corporation: Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-...

Due to a distribution error, product from the affected lot was shipped expired.

FDAMar 26, 2020Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Triton Canister System (finished part numbers FG 12009, f...

Some Canister Scanning Labels used to calibrate the Triton Canister System have a color variance. Based on a comprehensive analysis, blood loss estimates obtained using these Canister Scanning Labels may result in lower than expected results.

FDAJan 22, 2020Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: SafeAir Telescopic Smoke Evacuation Pencil, Product No. ...

Fire/Burn Risk

Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

1...3 456 7...14

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FDAJan 13, 2020Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Telescopic Smoke Evac Pencil, PB, Coated, Product No. SH...

Fire/Burn Risk

Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

FDAJan 13, 2020Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Telescopic Uncoated (Push Button), Product No. SHK TSPL....

Fire/Burn Risk

Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

FDAJan 13, 2020Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Corporation: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). O...

Sterile drapes packaged in an unsealed pouch.

FDAJan 7, 2020Nationwide• Stryker Corporation

Stryker Corporation: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold inter...

Sterile drapes packaged in an unsealed pouch.

FDAJan 7, 2020Nationwide• Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, ...

There is a potential for the cuff to leak air leading to a loss of vascular occlusion.

FDANov 6, 2019Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Corporation: Stryker, REF: 0250070450, 5.0 mm x 45 cm, Strykeprobe, Ou...

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.

FDASep 12, 2019PR• Stryker Corporation

Stryker Corporation: Stryker, REF: 0250070460, 5.0 mm x 32 cm, Strykeprobe, Ou...

FDASep 12, 2019PR• Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: C2 Nerve Monitor, 4 Channel, 5140-508-240, UDI 0761332717...

Stryker C2 NerveMonitor's design and instructions may not optimally address usability issues related to the functionality of the device, which may result in use errors potentially causing or contributing to nerve injury.

FDAJul 31, 2019Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: C2 Nerve Monitor, 8 Channel, 5140-508-280, UDI 0761332727...

FDAJul 31, 2019Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Corporation: Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Dou...

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.

FDAJul 19, 2019AK, AZ, AR +16 more• Stryker Corporation

Stryker Corporation: Stryker Connected OR Cart,120 V Ref Cat. #240-099-155, Qt...

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.

FDAApr 23, 2019Nationwide• Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Flyte Togas are components of the Stryker Flyte System an...

A single lot (11121171) of Flyte Toga Peel-away X-Large (catalog number 0408-830-100) was labeled with an incorrect expiration date of 2412-12-01. The correct expiration date should have read 2014-12-01.

Class IIILow

FDADec 22, 2014Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker SmartLife Large Aseptic Housing REF 7126-120-000...

The SmartLife Aseptic Housings are being recalled in that the top section of the housing may separate from the bottom section due to insufficient welding.

Class IIModerate

FDAOct 8, 2014Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker SmartLife Small Aseptic Housing REF 7222-120-000...

The SmartLife Aseptic Housings are being recalled in that the top section of the housing may separate from the bottom section due to insufficient welding.

Class IIModerate

FDAOct 8, 2014Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker CBCII Double Trocar/Double Pouch Kit with 3/16in....

The product may not be sterile due to package not being intact.

FDANov 12, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker CBCII Double Trocar Kit with 1/8 in. (3.2mm) Drai...

The product may not be sterile due to package not being intact.

FDANov 12, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker CBC ConstaVac Blood Conservation Kit 3/16in. (4.8...

The product may not be sterile due to package not being intact.

FDANov 12, 2009Nationwide• Stryker Instruments Div. of Stryker Corporation