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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 34841–34860 of 37665 recalls

Stryker Instruments Div. of Stryker Corporation: Stryker PainPump1 2-Site Y-Connector; Product number 500-...

The catheter tubing included in the kit may break during removal.

FDAFeb 3, 2006Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker PainPump1.5 2-Day Infusion Kit; Product number 50...

The catheter tubing included in the kit may break during removal.

FDAFeb 3, 2006Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker PainPump1 1-Day Infusion Kit; Product number 500-...

The catheter tubing included in the kit may break during removal.

FDA

1...1741 174217431744 1745...1884

Page 1743 of 1884Next

Feb 3, 2006

Nationwide

• Stryker Instruments Div. of Stryker Corporation

Fujifilm Medical System USA, Inc.: Synapse Software Versions 3.1.0 and 3.1.1 used with the F...

Image orientation and orientation markers may not match when an image is rotated or flipped when the CT Image is preset.

FDAFeb 3, 2006Nationwide• Fujifilm Medical System USA, Inc.

Stryker Instruments Div. of Stryker Corporation: Stryker PainPump1 Base Kit; Product number 500-100-000.

The catheter tubing included in the kit may break during removal.

FDAFeb 3, 2006Nationwide• Stryker Instruments Div. of Stryker Corporation

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Paceart 2004 Second Edition & Paceart 2005 Firs...

The Paceart System could inappropriately insert data from a patient's Medtronic CareLink transmission into another patient's Paceart record. An issue associated with the automated batch transfer of implanted cardiac device data from the Medtronic CareLink network to the Paceart System exists.

FDAFeb 2, 2006Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Baby Walkers (SunTome) – Stairway Fall Risk (2006)

The recalled walkers have eight wheels and are sold in various colors including dark blue, pink and white, or pink and red. The activity trays on the baby walkers have a steering wheel, various rattles and a mirror or animal themes. The trays play music when the baby pushes a button. "Baby" is printed on a sticker on the tray or the walker's base.

CPSCFeb 1, 2006Nationwide• SunTome Trading Corp., of Los Angeles, Calif.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 500 automated external defibrillator (AED)

Component leads may have intermittent connection to the printed circuit board assembly pads - which could render the device inoperative.

FDAFeb 1, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK EXPRESS defibrillator

One of the printed circuit board assemblies may be contaminated with solder flux which can cause a short that may render the device inoperative.

FDAJan 31, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK CR Plus defibrillator

One of the printed circuit board assemblies may be contaminated with solder flux which can cause a short that may render the device inoperative.

FDAJan 31, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Hitachi Medical Systems America Inc: Hitachi Altaire Magnetic Resonance Imaging System

Circuit Failure-There is the potential risk of the Phase Loss Detector Safety Device (PHSEN PCB) malfunctioning in the event of a power loss. The circuit may fail to turn off the system main breaker when 2 of the 3 power phases are lost.

FDAJan 27, 2006Nationwide• Hitachi Medical Systems America Inc

General Electric Med Systems LLC: Discovery ST PET/CT imaging system with gantry model numb...

The LightSpeed CT Technical Reference Manual was omitted from the document kit shipped with the PET/CT system.

FDAJan 26, 2006Nationwide• General Electric Med Systems LLC

Tosoh Bioscience Inc: TOSOH ST AIA- PACK TT3, Lot FX17440, catalog #025...

The inner foil packs of AIA-PACK ST TT3, Lot FX17440 contain an incorrect expiration date of 10/2005. The outer box is labeled with the correct expiration date of 10/2006.

FDAJan 26, 2006GA, KS, TX +1 more• Tosoh Bioscience Inc

RC2 Brands Inc., The First Years: The First Years Cool Animal Teether/Fish, Zebra and Dinos...

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

RC2 Brands Inc., The First Years: Disney Baby Soft Cool Ring Teether Style # Y1470

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

RC2 Brands Inc., The First Years: Sesame Beginnings Chill & Chew Teether Style #Y3095

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

Medtronic Sofamor Danek Instrument Manufacturing: METRx II Tube, 14mm x 8cm stainless steel tubular retract...

Due to a manufacturing error after autoclaving, the Tubular Retractor coating, Physical Vapor Deposition (PVD) black Titanium Nitride (TiN), may rub off.

FDAJan 25, 2006CA, IL, IN +1 more• Medtronic Sofamor Danek Instrument Manufacturing

Medtronic Sofamor Danek Instrument Manufacturing: METRx II Tube, 14mm x 3cm stainless steel tubular retract...

Due to a manufacturing error, after autoclaving, the Tubular Retractor coating, Physical Vapor Deposition (PVD) black Titanium Nitride (TiN), may rub off.

FDAJan 25, 2006CA, IL, IN +1 more• Medtronic Sofamor Danek Instrument Manufacturing

RC2 Brands Inc., The First Years: The First Years Floating Friend Teether Style #Y1474

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

Medtronic Sofamor Danek Instrument Manufacturing: METRx II Tube, 18mm x 3cm stainless steel tubular retract...

Due to a manufacturing error after autoclaving the Tubular Retractor coating, Physical Vapor Deposition (PVD) black Titanium Nitride (TiN), may rub off.

FDAJan 25, 2006CA, IL, IN +1 more• Medtronic Sofamor Danek Instrument Manufacturing