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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

1000

Past Year

1000

Class I (Serious)

143

Most Recent

Jan 2026

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 32121–32140 of 37665 recalls

Stryker Instruments Div. of Stryker Corporation: Stryker PainPump2, 400 mL PainPump with 2.5 inch ExFen 2 ...

An electronic failure during preparation of the unit, or during patient use, may cause the pump to shut down.

FDAFeb 11, 2009AL, AK, AZ +43 more• Stryker Instruments Div. of Stryker Corporation

Arrow International Inc: Arrow Balloon and stylet temporary pacing catheter

Leakage: Material not lipid resistant, may crack and/or leak. Use of this device with lipid containing solutions or 70% isopropyl alcohol may cause leakage or air embolism.

FDAFeb 11, 2009Nationwide• Arrow International Inc

Arrow International Inc: Arrow Multi-Lumen CVC w/ BlueFlex Tip (Central Venous Cat...

Leakage: Material not lipid resistant, may crack and/or leak. Use of this device with lipid containing solutions or 70% isopropyl alcohol may cause leakage or air embolism.

1...1605 160616071608 1609...1884

Page 1607 of 1884Next

FDA

Feb 11, 2009

Nationwide

• Arrow International Inc

Arrow International Inc: Arrow Single Lumen CVCs (Central Venous Catheters)

Leakage: Material not lipid resistant, may crack and/or leak. Use of this device with lipid containing solutions or 70% isopropyl alcohol may cause leakage or air embolism.

FDAFeb 11, 2009Nationwide• Arrow International Inc

Cooking Systems (Jetboil) – burn hazard (2009)

Fire/Burn Risk

This recall involves personal and group cooking stoves often used during outdoor camping. The recalled models include: Personal Cooking Systems in black (PBL075-BLK-(PCS) and camo (PBL075-CAMO-(PCS), Backcountry Gourmet Set (BDLFRY), Personal Cooking System with Companion Cup (BDL001), Personal Cooking System with Pot Support & Stabilizer (BDL002), Personal Cooking System with Coffee Press (BDL003), and Personal Cooking System Java Kit (BDLJAVA) and Group Cooking System (GCS150).

CPSCFeb 11, 2009Nationwide• Jetboil Inc., of Manchester, N.H.

Arrow International Inc: Arrow 4way Hi-Flo Stopcock with male luer lock, latex fre...

Leakage: Material not lipid resistant, may crack and/or leak. Use of this device with lipid containing solutions or 70% isopropyl alcohol may cause leakage or air embolism.

FDAFeb 11, 2009Nationwide• Arrow International Inc

Arrow International Inc: Arrow Super Arrow-Flex Percutaneous Sheath Introducers

Leakage: Material not lipid resistant, may crack and/or leak. Use of this device with lipid containing solutions or 70% isopropyl alcohol may cause leakage or air embolism.

FDAFeb 11, 2009Nationwide• Arrow International Inc

Stryker Instruments Div. of Stryker Corporation: Stryker PainPump2, 250 mL PainPump with Luer Lock Tubing ...

An electronic failure during preparation of the unit, or during patient use, may cause the pump to shut down.

FDAFeb 11, 2009AL, AK, AZ +43 more• Stryker Instruments Div. of Stryker Corporation

Synthes Spine: Synthes Zero-P StarDrive Screwdriver Shaft, T8, self-reta...

Tip breakage, due to inadequate instructions for use. The Technique Guide provided incorrect information related to use of the Torque Limiting Attachment during screw insertion and final tightening.

FDAFeb 10, 2009Nationwide• Synthes Spine

Golfer's Billiard Games (Golf Gifts) – Lead Paint Violation (2009)

The recalled golfer's billiard game includes 15 golf balls (with exterior paint and design to resemble a billiard ball) and six putting cups. The recall involves the Acuity Golfer's Billiard Game, Style #AC302, and the Clubhouse Golfer's Billiard Game, Style #302. The name and style number are located on the product's packaging.

CPSCFeb 10, 2009Nationwide• Golf Gifts and Gallery, of Powers Lake, Wisc.

Bicycle Forks (Marzocchi) – Crash Risk (2009)

The recalled bicycle forks were sold for installation on mountain bikes. The recall involves certain 2008 model year 888RC3 and 888RC3WC suspensions with date codes beginning with T07D07, T07D08 and T07D09. The forks are white or black with red and black artwork on the legs.

CPSCFeb 10, 2009Nationwide• Tenneco-Marzocchi s.r.l., of Bologna, Italy

Synthes USA (HQ), Inc.: NFix II System 150mm The Synthes N-Hance and NFix II rods...

package integrity compromised

FDAFeb 9, 2009AL, AK, AZ +32 more• Synthes USA (HQ), Inc.

Synthes USA (HQ), Inc.: TI N-Hance Rod 150mm Sterile The Synthes N-Hance and NFix...

package integrity compromised

FDAFeb 9, 2009AL, AK, AZ +32 more• Synthes USA (HQ), Inc.

Synthes USA (HQ), Inc.: NFlex Straight monosegmental L 150mm The Synthes N-Hance ...

package integrity compromised

FDAFeb 9, 2009AL, AK, AZ +32 more• Synthes USA (HQ), Inc.

Synthes USA (HQ), Inc.: NFlex Stabilization System 150mm The Synthes N-Hance and ...

package integrity compromised

FDAFeb 9, 2009AL, AK, AZ +32 more• Synthes USA (HQ), Inc.

Synthes USA (HQ), Inc.: N-Hance System 150mm The Synthes N-Hance and NFix II rods...

package integrity compromised

FDAFeb 9, 2009AL, AK, AZ +32 more• Synthes USA (HQ), Inc.

Synthes Spine: Square Nut MR Safe, Catalog Number 03.311.060. The Squa...

Numbers are etched incorrectly on the product.

FDAFeb 9, 2009AR, CA, CO +17 more• Synthes Spine

Medtronic Sofamor Danek USA Inc: Medtronic INTREPID Spinal System SPACER, 32X23, 8 DEG, Si...

The firm received complaints regarding the use of the product in patients with poor bone quality, translational instability, difficulty implanting the cover plate and case of cover plate detachment.

FDAFeb 6, 2009Nationwide• Medtronic Sofamor Danek USA Inc

Biosite Inc: Triage Total Controls Calibration Verification 5: Two - 0...

Incidence of low recovery results has exceeded post market surveillance thresholds of customer complaints in the field.

FDAFeb 6, 2009Nationwide• Biosite Inc

Computerized Medical Systems Inc: Focal Radiation Treatment Planning System, Focal Release...

Focal Software: if individual MLC leaf position edits are made, the original MLC aperture is retained. A subsequent aperture edit should not affect the MLC leaf positions however it was found that instead the leaves will then snap (unintentionally) back to the original aperture. Also, if the patient is sent to XiO after the MLC is edited, an isocenter shift made in XiO will also cause the MLCs to

FDAFeb 6, 2009Nationwide• Computerized Medical Systems Inc