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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 32861–32880 of 37665 recalls

Stryker Instruments Div. of Stryker Corporation: Stryker Ortholock EX Pin for use with the Stryker Navigat...

Laceration Risk

Instructions have been updated to include new warnings regarding percutaneous pin placement during surgery in order to mitigate the risk of femur fractures.

FDAJun 5, 2008Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker Ortholock, Stryker, Kalamazoo, MI; Part 6007-003-...

Laceration Risk

Instructions have been updated to include new warnings regarding percutaneous pin placement during surgery in order to mitigate the risk of femur fractures.

FDAJun 5, 2008Nationwide• Stryker Instruments Div. of Stryker Corporation

Mini Chef Toy Kitchens (eStyle) - Choking Hazard (2008)

1...1642 164316441645 1646...1884

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Choking Hazard

The Mini Chef Complete Kitchen is a wooden unit with a metal sink, faucet, four-burner stove with front oven and five-turn-knob control panel, refrigerator, shelves, phone, clock, microwave door and roof. The recalled toy kitchen is approximately 32 inches by 43 inches.

CPSCJun 5, 2008Nationwide• eStyle Inc., of Los Angeles, Calif.

Simmons Kids Crib Mattresses (Simmons Kids) – entrapment risk (2008)

The recalled mattresses involve open coil crib mattresses manufactured between July 1, 2006 and March 23, 2008 with a color label attached to the top or side of the mattress that has the following model names: Pottery Barn Kids by Simmons Kids Lullaby Simmons Kids Slumber Time Evening Star Luxury Firm Simmons Kids Baby Mattress Series 400 Simmons Kids Baby Mattress 234 Coil Count The crib mattresses also have a law tag that is sewn into the edge of the mattress. The law tag has the date of manufacture and in most cases will contain one of the following model numbers: H59044.15.0014, M59082.15.0002, M59027.15.0002 or M59065.15.0006. Pocketed Coils® and Simmons Kids or Simmons Juvenile Products crib mattresses manufactured before July 1, 2006 or after March 23, 2008 are not included in the recall.

CPSCJun 5, 2008Nationwide• Simmons Kids, a division of The Simmons Manufacturing Co., LLC of Atlanta, Ga.

Medtronic Neuromodulation: PROSTIVA RF Model 8929 Hand Piece is the delivery system ...

Reported incidents of needle retraction failure when using the PROSTIVA RF Model 8929 Hand Piece. The Medtronic Prostiva RF Model 8929 Hand Piece is the delivery system component of the PROSTIVA RF Therapy System.

FDAJun 5, 2008AL, AZ, AR +44 more• Medtronic Neuromodulation

Cardinal Health NeuroCare Division: NicoletOne photic adapter cable 085-463700

Cardinal Health NeuroCare is implementing a voluntary field correction to replace a quantity of photic adapter cables, part number 085-463700, used to connect the NicLED Photic Strobe option, part number 698-625500, with NicoletOne EEG system. The photic adapter cable has a wiring error which delivers a reduced voltage and results in a decreased intensity of the NicLED photic. This reduced intensi

FDAJun 5, 2008CA, FL, GA +14 more• Cardinal Health NeuroCare Division

Orthosoft, Inc. dba Zimmer CAS: Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plas...

Zimmer CAS voluntarily conducted a retrospective recall of the Sesamoid Plasty due to the risk of the top of the workstation to potentially fall over during disassembly.

FDAJun 4, 2008CA, FL• Orthosoft, Inc. dba Zimmer CAS

Polaris ATVs - Fire Hazard (2008)

Fire/Burn Risk

This recall involves the Polaris ATVs with model year 2004 and model numbers listed below that have been serviced for electrical problems and received a defective EMC during service work. The ATVs were sold under market names Scrambler 500 and Sportsman 400, 500, or 6 x 6. The model number is printed on a decal attached to the front side of the radiator (Sportsman) or the top of the front cab cover (Scrambler 500). Model Year Model Market Name 2004 A04BG50AA Scrambler 500 4x4 2004 A04BG50FA Scrambler 500 2004 A04CH42AQ Sportsman 400 2004 A04CH42AR Sportsman 400 2004 A04CH42AS Sportsman 400 2004 A04CH42AT Sportsman 400 2004 A04CH42AV Sportsman 400 2004 A04CH50AO Sportsman 500 2004 A04CH50AQ Sportsman 500 2004 A04CH50AR Sportsman 500 2004 A04CH50AS Sportsman 500 2004 A04CH50AT Sportsman 500 2004 A04CH50AV Sportsman 500 2004 A04CH50AW Sportsman 500 2004 A04CH50AX Sportsman 500 2004 A04CL50AA Sportsman 6x6

CPSCJun 4, 2008Nationwide• Polaris Industries Inc., of Medina, Minn.

Orthosoft, Inc. dba Zimmer CAS: Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Pla...

Zimmer CAS voluntarily conducted a retrospective recall of the Sesamoid Plasty due to the risk of the top of the workstation to potentially fall over during disassembly.

Class IIModerate

FDAJun 4, 2008CA, FL• Orthosoft, Inc. dba Zimmer CAS

GE Medical Systems, LLC: GE Healthcare, Infinia Hawkeye 4, Model Numbers: 5178728,...

The metal pin in the adjustable head holder, which is used to acquire Brain SPECT data on Infinia systems (Infinia, Infinia Hawkeye, and Infinia Hawkeye 4), creates an artifact on the patient's cerebellum, which may lead to the potential for misdiagnosis.

FDAJun 2, 2008AL, AK, AZ +44 more• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Healthcare Infinia, Model Numbers: ASM000886, ASM0013...

GE Healthcare has recently became aware of excessive pressure applied by the collimator pressure sensitive cover of Infinia (Infinia, Infinia Hawkeye, Infinia Hawkeye 4) that may impact patient safety. It was reported at a customer site that the pressure used to activate the Pressure Sensitive Device (PSD) should be lowered and that the body contouring software requires correction to prevent po

FDAJun 2, 2008AL, AK, AZ +44 more• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Healthcare, Hawkeye for Infinia, Model Numbers: H3000W...

FDAJun 2, 2008AL, AK, AZ +44 more• GE Medical Systems, LLC

Abbott Laboratories: AxSYM Rubella IgG Reagent Pack; Abbott Laboratories, Abbo...

An increase in complaints was noted for AxSYM Rubella IgG assay calibration failures due to error codes related to elevated Calibrator A (or Master Calibrator 1) rates too high.

FDAJun 2, 2008PR• Abbott Laboratories

GE Medical Systems, LLC: GE Healthcare Infinia Hawkeye, Model Numbers: H3000WR, H3...

FDAJun 2, 2008AL, AK, AZ +44 more• GE Medical Systems, LLC

Varian Medical Systems Oncology Systems: Varian RV Software Varian Treatment for Non-Varian Linacs...

A malfunction within the Varis software might result in a misadministration (underdose). The software does not correctly interpret the number, causing field parameters having decimal values to be incorrect.

FDAJun 2, 2008Nationwide• Varian Medical Systems Oncology Systems

GE Medical Systems, LLC: GE Healthcare, Infinia, Model Numbers: ASM000886 ASM0013...

FDAJun 2, 2008AL, AK, AZ +44 more• GE Medical Systems, LLC

Intuitive Surgical, Inc.: da Vinci S Surgical System, Model number IS2000 Endoscopi...

Defective software chip may cause the system to fail and lock up.

FDAJun 1, 2008Nationwide• Intuitive Surgical, Inc.

Medtronic Powered Surgical Solutions: Medtronic Midas Rex Legend tapered dissecting tool, Model...

Laceration Risk

Cutting flute geometry of surgical dissecting tools may be outside of established tolerance. This may lead to reduced cutting performance, inability to perform desired dissection, increased risk of overheating, and potential need for revision surgery.

FDAMay 30, 2008Nationwide• Medtronic Powered Surgical Solutions

Polymer Technology Systems, Inc.: PTS Panels LDL Cholesterol test strips for professional u...

The expiration date was extended by 20 weeks without justification.

FDAMay 29, 2008Nationwide• Polymer Technology Systems, Inc.

Beckman Coulter Inc: COULTER LH SlideMaker, LH Barcode Specification, LH SM In...

Beckman Coulter has become aware of a potential issue in which the Sample ID information embedded in the barcode affixed to a slide made by the Coulter GEN*S and LH SlideMaker does not match the text.

FDAMay 29, 2008Nationwide• Beckman Coulter Inc