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Rossignol Ski Company, Inc. and Skis Dynastar, Inc. of Williston, Vermont

Rossignol Ski Company, Inc. and Skis Dynastar, Inc. of Williston, Vermont Recalls

All product recalls associated with Rossignol Ski Company, Inc. and Skis Dynastar, Inc. of Williston, Vermont.

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Recall Summary

Total Recalls

1000

Past Year

620

Class I (Serious)

Most Recent

Dec 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 10401–10420 of 10937 recalls

Snowboard Bindings (Rossignol/Dynastar) – safety failure (2005)

This recall includes all 2003/2004 model year Rossignol-brand HC 500, Zena, Unit Pack, HC Rental, and Unit Rental snowboard bindings. Also included are the 2003/2004 model year Dynastar-brand Classic RL and Classic Pack snowboard bindings. This recall does not involve current products (2004-2005) or other models.

CPSCFeb 1, 2005Nationwide• Rossignol Ski Company, Inc. and Skis Dynastar, Inc. of Williston, Vermont

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; 100V -120V, 15 A (cir...

System 1 power supply may electrically short to the main console, disrupting normal system operation by causing unexpected re-setting or shutdown of pumps and modules, false alarms and/or overheating and failure of the central control monitor.

FDAFeb 1, 2005Nationwide• Terumo Cardiovascular Systems Corp

Guidant Corporation Advanced CardiovascularSystem: Voyager RX Coronary Dilatation Catheter

1...519 520521522 523...547

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Leak at guide wire exit notch could introduce air into the artery.

FDAJan 27, 2005IN• Guidant Corporation Advanced CardiovascularSystem

GE OEC Medical Systems, Inc: InstaTrak 3500 Plus system with cranial application (aid ...

Tracking inaccuracy of 5-10 mm may result when the shunt guide accessory is used with version 5.1 software.

FDAJan 26, 2005AL, AK, AZ +21 more• GE OEC Medical Systems, Inc

Jumpking Trampolines (Jumpking Inc.) – Potential Injury Risk (2005)

Laceration Risk

The recall includes 14-foot and 15-foot Jumpking trampolines sold separately and with FunRing enclosures. The brand name "Jumpking, Inc." is written on a warning label wrapped around a leg of the trampoline. The eight legs of these trampolines fit into perpendicular sockets welded to the top rails. Trampolines with weldless sockets that fit over the connecting top rail pieces are not included in this recall. The FunRing enclosures have an arched design where the vertical poles are connected by arches at the top. Some enclosures were sold separately from the trampolines. Later units, that include the rubber sleeves that fit around the mounting brackets, are not included in the recall.

CPSCJan 25, 2005Nationwide• Jumpking Inc.® of Mesquite, Texas

Fun Years Music Big Drum Set (Kids Station) – Potential Injury (2005)

Choking Hazard

The recalled music set includes a yellow and green drum with a clear plastic lid and a red one-piece carrying strap that doubles as a storage and carrying case for additional instruments. The drum measures 12 inches in diameter and about 7.5 inches in height. The instruments stored in the drum include: purple drumsticks, yellow and red dumb-bell-shaped maracas, purple wrist bells, an orange recorder, a yellow harmonica, a red-rimmed tambourine and a yellow whistle. Only this musical set is part of this recall. A similar drum set sold at Toys "R" Us with a two-piece strap and different musical toys is manufactured by a different company and is not being recalled.

CPSCJan 19, 2005Nationwide• Kids Station Inc., of Miami, Fla., for Toys "R" Us, of Wayne, N.J.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 12 defibrillator/ monitors biphasic

The LIFEPAK 12 biphasic defibrillator/ monitors may deliver inappropriate energy levels and fail to escalate energy levels when configured to do so.

FDAJan 15, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Fischer Imaging Corporation: Bloom DTU-215-B Programmable Stimulator

Possibility that after a loss of power or brown-out, the device may transmit unintended stimulation to patients.

FDAJan 13, 2005Nationwide• Fischer Imaging Corporation

LMS Medical Systems Ltd: CALM software, version 02.09.01 This software is intend...

A deficiency in the software code can, in certain circumstances, cause data for the wrong patient to be displayed in the Tracing Review screen when a user is acknowledging an Alert

FDAJan 11, 2005AL, IL, MD +2 more• LMS Medical Systems Ltd

Smiths Medical PM, Inc.: Advisor Vital Signs Monitor model 9200, catalog number 92...

An issue with the pace detect function was discovered on a 9200 II monitor. Could result in a falsely high or low heart rate reading.

FDAJan 5, 2005Nationwide• Smiths Medical PM, Inc.

Northwest Medical Physics Equipment Inc: ISOLOC Software Version 6.0, Part Number NT-NW-425-520. ...

When ISOLOC version 6.0 software was used in the Anatomic Landmark mode, the couch moves display in the Couch Translator window was incorrect.

FDADec 30, 2004Nationwide• Northwest Medical Physics Equipment Inc

General Electric Med Systems LLC: Precision 500D Radiographic/Fluoroscopic X-ray System, mo...

Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur.

FDADec 30, 2004Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: Proteus XR/a Radiographic X-ray System, models 2259973-1,...

Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur.

FDADec 30, 2004Nationwide• General Electric Med Systems LLC

Philips Medical Systems Sales & Service Region No. America: Xcelera R1.2 Cardiology image and information management ...

Loss of image data from image repository and archive requiring patients to undergo repeat imaging.

FDADec 21, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Metallic Children's Necklaces (Raymond Geddes) – Choking Risk (2004)

Laceration Risk

The recalled necklaces have medallions that came in four different designs, depicting frogs, dolphins with a small bead on the tail, a sunshine smiley face and an alien face on a starburst. The medallion is on a black rope chain surrounded by a metallic bead with a coil section.

CPSCDec 17, 2004Nationwide• Raymond Geddes Co. Inc., of Baltimore, Md.

Philips Medical Systems: Philips Heartstart MRx Monitor/Defibrillator Models: M35...

In Software versions below A.02.00, with the sync function enabled and the device switched from manual to AED, there may be an unexpected delay in delivery of energy

FDADec 15, 2004Nationwide• Philips Medical Systems

OEC Medical Systems, Inc: InstaTrak 3500 Plus Navigation and Visualization System

Enhanced sterility testing revealed the sterilization efficacy of accessories ('Sensors') used with certain Navigation and Visualization systems may be compromised.

FDADec 13, 2004Nationwide• OEC Medical Systems, Inc

OEC Medical Systems, Inc: ENTrak Navigation and Visualization System

Enhanced sterility testing revealed the sterilization efficacy of accessories ('Sensors') used with certain Navigation and Visualization systems may be compromised.

FDADec 13, 2004Nationwide• OEC Medical Systems, Inc

OEC Medical Systems, Inc: ENTrak Plus Navigation and Visualization System

Enhanced sterility testing revealed the sterilization efficacy of accessories ('Sensors') used with certain Navigation and Visualization systems may be compromised.

FDADec 13, 2004Nationwide• OEC Medical Systems, Inc

OEC Medical Systems, Inc: InstaTrak 3000 Navigation and Visualization System

Enhanced sterility testing revealed the sterilization efficacy of accessories ('Sensors') used with certain Navigation and Visualization systems may be compromised.

FDADec 13, 2004Nationwide• OEC Medical Systems, Inc