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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 33181–33200 of 37665 recalls

Stryker Instruments Div. of Stryker Corporation: Stryker VertePort , 11 G Cement Cannula, REF 306-510 , Q...

Mis-labeing; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy)

FDAFeb 13, 2008Nationwide• Stryker Instruments Div. of Stryker Corporation

Varian Medical Systems Oncology Systems: Eclipse Treatment Planning System, Client 8.1.18 and DCF ...

A software error causes the wedge accessory calculation to be ignored in the radiotherapy treatment plan.

FDAFeb 13, 2008AL, AZ, AR +24 more• Varian Medical Systems Oncology Systems

Abbott Spine: Sequoia Spinal System Surgical Kits; Pedicle screw spinal...

Screw Head Dissociation: The polyaxial screw head may dissociate from screw shaft during surgery. Also, the polyaxial screw driver is experiencing difficulty (broken/bent driver shafts, difficulty attaching screws to the driver and jamming of the collet.)

1...1658 165916601661 1662...1884

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FDAFeb 13, 2008Nationwide• Abbott Spine

Stryker Instruments Div. of Stryker Corporation: Stryker VertePort, 10 G Cement Cannula, REF 306-410, Qty...

Mis-labeling; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy)

FDAFeb 13, 2008Nationwide• Stryker Instruments Div. of Stryker Corporation

International Technidyne Corp.: International Technidyne Corp. (ITC) AVOXimeter 1000 Oxi...

Incorrect reading: ITC discovered that instruments built or repaired since approximately April 2007 were inadvertently left with the diagnostic mode enabled when shipped to customers.

FDAFeb 13, 2008Nationwide• International Technidyne Corp.

Advanced Sterilization Products: EvoTech Endoscope Cleaner and Reprocessor, Product Code 5...

Cleaning cycles are being cancelled. Specific issues are: a) Water heater tank is rusting resulting in the in-line 0.2 micron filter prematurely clogging, b) Interface board malfunction resulting in a premature lid opening, and c) Minor fluid leaks within the system (commonly at the 0.2 micron filter attachment points).

FDAFeb 13, 2008Nationwide• Advanced Sterilization Products

Stryker Instruments Div. of Stryker Corporation: Stryker VertePort, 10 G Access Cannula w/Long Stylet Syst...

Mis-labeling; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy)

FDAFeb 13, 2008Nationwide• Stryker Instruments Div. of Stryker Corporation

Chattem Inc: Aspercreme, Pain Relieving Creme with Aloe, Maximum Stren...

Fire/Burn Risk

Skin irritation and burns with product usage

FDAFeb 12, 2008Nationwide• Chattem Inc

Chattem Inc: Icy Hot Heat Therapy , Air Activated Heat Patch, Back and...

Fire/Burn Risk

Skin irritation and burns with product usage

FDAFeb 12, 2008Nationwide• Chattem Inc

GE Gas Dryers - Shock Hazard (2008)

The recalled gas dryers are 42 inches tall (back with backsplash) and 27 inches wide, and were sold in white. GE gas dryers model number DWXR463GGWW with serial numbers starting with AM, TL, SL, VL, and ZL are included in this recall. To find the model and serial numbers, open the dryer door and look in the lower right corner, in the area that was covered by the door.

CPSCFeb 11, 2008Nationwide• GE Consumer & Industrial, of Louisville, Ky.

Hitachi Medical Systems America Inc: Altaire MRI System Emergency Rundown Switch Unit (ERDU) i...

The firm's Altaire MR Scanner's Emergency Rundown Switch Unit (ERDU), that is used to shut down the device in an emergency, was found to be defective. An ERDU failure could delay or prevent patient access leading to possible patient death or serious injury.

FDAFeb 11, 2008Nationwide• Hitachi Medical Systems America Inc

Pointe Scientific, Inc.: Liquid Alk Phos R2 Reagent, Catalog No. 3-A7516-R2, In v...

May be contaminated with microorganisms.

FDAFeb 7, 2008Nationwide• Pointe Scientific, Inc.

Pointe Scientific, Inc.: Liquid Alkaline Phosphatase (R2) Reagent Set, Catalog No....

May be contaminated with microorganisms.

FDAFeb 7, 2008Nationwide• Pointe Scientific, Inc.

Boston Scientific Corporation One Boston: Boston Scientific Mach 1 Guide Catheter 6F, IM Internal M...

Mislabeled: Seven lots/ batches of Boston Scientific Mach 1 Guide Catheter may be mislabeled with the incorrect device length.

FDAFeb 7, 2008AL, AZ, AR +21 more• Boston Scientific Corporation One Boston

Pointe Scientific, Inc.: Liquid Alkaline Phosphatase Reagent Set, Catalog Nos. A75...

May be contaminated with microorganisms.

FDAFeb 7, 2008Nationwide• Pointe Scientific, Inc.

Pointe Scientific, Inc.: Liquid Alk Phos Reagent, Catalog No. 3-A7516-L, In vitro ...

May be contaminated with microorganisms.

FDAFeb 7, 2008Nationwide• Pointe Scientific, Inc.

Transparent Egg Shakers (West Music) - Choking Risk (2008)

Choking Hazard

This recall involves clear, plastic egg-shaped instruments with various color beads inside. The beads inside the shaker instrument come in five colors: red, white, green, dark blue and aqua. "Basic Beat" and "Jumbo Egg Crystal" is printed on a label attached to the plastic bag packaging. Model numbers "BB5102" and "202212" are printed on the side of the label.

CPSCFeb 7, 2008Nationwide• West Music Company, of Coralville, Iowa

Pointe Scientific, Inc.: Alk Phos R1 (also labeled as Alkaline Phosphatase R1) Rea...

May be contaminated with microorganisms.

FDAFeb 7, 2008Nationwide• Pointe Scientific, Inc.

Stryker Endoscopy: Stryker Wedge HS Suture Anchor II with Needles, 5.0 mm, M...

Product package may crack and cause loss of sterility.

FDAFeb 7, 2008CA, CO, IN +4 more• Stryker Endoscopy

Boston Scientific Corporation One Boston: Boston Scientific Mach 1 peripheral Guide Catheter 6F, H...

Mislabeled: Seven lots/ batches of Boston Scientific Mach 1 Guide Catheter may be mislabeled with the incorrect device length.

FDAFeb 7, 2008AL, AZ, AR +21 more• Boston Scientific Corporation One Boston