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Nicolet Biomedical Div of Viasys Healthcare

Nicolet Biomedical Div of Viasys Healthcare Recalls

All product recalls associated with Nicolet Biomedical Div of Viasys Healthcare.

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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 34421–34440 of 37665 recalls

Nicolet Biomedical Div of Viasys Healthcare: NicoletOne version 5.20 software (also known as NicoletOn...

A software anomaly exists in the 5.20.1038 NicoletOne LTM, Sleep, nEEG, vEEG and ICU Monitor systems using the M, and/or C series amplifiers. If this anomaly occurs, the system will display the data for channel one in all channels on NicoletOne LTM, Sleep, nEEG, vEEG or ICU Monitor systems.

FDAAug 25, 2006Nationwide• Nicolet Biomedical Div of Viasys Healthcare

Thoratec Corp: Thoratec brand TLC-II Portable Ventricular Assist Device ...

Sticky Valve Disk- The valve disk has an increased tendency to stick during operation causing noise and pressure/vacuum alarms.

FDAAug 25, 2006AL, CA, CT +18 more• Thoratec Corp

Philips Medical Systems North America Co. Phillips: Allura Xper FD 10 x-ray, angiographic system

Potential for x-ray system to freeze during an examination, and inability of table to be re-positioned.

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FDAAug 24, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD 10/10 x-ray, angiographic system

Potential for x-ray system to freeze during an examination, and inability of table to be re-positioned.

FDAAug 24, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Bemis Health Care, Inc: 5 Qt. Wallmount Sharps Container, Model 150, Regular Size...

The 5 Quart Wall Safes are shipped as two pieces (bottom & top) that customers are unable to assemble because of excess warp in the back wall of the container.

FDAAug 23, 2006Nationwide• Bemis Health Care, Inc

Fire Suppression Pumps (ITT) – system failure (2006)

Fire/Burn Risk

The recalled pumps are general in purpose, but are sometimes used in fire suppression systems. The pumps were sold under the Goulds Pumps, Bell & Gossett and Red Jacket Water Products brands. The pumps can be identified by having Model NPE, NPO, MCC, MCS, SM or Series 3530 on their nameplate. Recalled pumps were manufactured between December 2005 and July 26, 2006. They have date code M05, A06, B06, C06, D06, E06, F06 or G06. The date code is the first three digits of the serial number on the pump nameplate.

CPSCAug 23, 2006Nationwide• ITT Water Technology Inc., of Auburn, N.Y.

Lawnmower Blades (Blount) – replacement defect (2006)

Laceration Risk

The recalled replacement lawnmower blades are intended for use on Snapper riding lawnmowers. The recalled blades are sold for use as replacement parts under the Oregon® and Silver Streak® brands only. Original equipment blades on Snapper lawnmowers and "Snapper" brand replacement blades are not included in this recall. The recalled blades are red and marked "MADE IN USA," "GRASS SIDE CX", "Oregon" or "SILVER STREAK." The part number and date code are engraved on one side of the blade. The recalled blades are part numbers: 99-111, 99-112, 99-113, 99-114, 99-117, 99-118, 99-926, 99-930 and date codes: BL, BM, BN, BP, BQ, BR, BS, BT, BU, BV, BW, BX, BY, BZ, CA, CB, CC, CD, CE, CF, CG, CH, CJ, CK, CL, CM, CN, CP.

CPSCAug 23, 2006Nationwide• Blount International Inc., of Kansas City, Mo.

Air Hogs RC Airplane (Spin Master) – burn hazard (2006)

Fire/Burn Risk

The recalled radio-controlled toy airplane is lightweight, made of silver or black Styrofoam, and measures 19 inches from wingtip to wingtip. "Air Hogs Skywinder" is printed on the plane's wings. "©2003 Spin Master Ltd" is printed on the right propeller mount. The airplane comes with a controller unit and a charger. Rechargeable batteries are preinstalled in the plane's fuselage. A date code beginning with 06XXXXHM is located under the plane's propeller, on the outside of the controller unit and inside the controller's battery compartment, and on the charger unit's stand.

CPSCAug 22, 2006Nationwide• Spin Master Toys, of Toronto, Canada

Firestreet Scooters (Triple Win) – fall hazard (2006)

Fire/Burn Risk

This recall involves F Forward Firestreet scooters. The red or blue aluminum scooters have a fold-down frame and model number BZ 020 SP. The "F Forward" logo is noted on the stem, wheel or base deck of the scooter.

CPSCAug 17, 2006Nationwide• Triple Win Sports, of Taiwan

Cage Bell Musical Instrument (Kindermusik) – choking risk (2006)

Choking Hazard

The musical instrument is a wooden cylinder with end caps and wooden dowels connecting the caps. A single bell is in the middle. Model number 5-30-00740 is sold individually; Model number 0-06-09005 is sold as part of a kit called Busy Days Home, which also contains a board book, a compact disc and a poster. The model number is written on the outside packaging of the product.

CPSCAug 17, 2006Nationwide• Kindermusik International Inc., of Greensboro, N.C.

Datex Ohmeda, Inc: GE Healthcare Innova 3100 IQ Digital Fluoroscopic Imaging...

User was unable to hear the Innova 2100-IQ 5-minute fluoroscopy warning signal from the Table Control TSSC interface. Inability of the user to hear the audible signal indicating the completion of any preset exposure time may lead to incorrect overall dose management, resulting in unnecessary exposure and can be a contributing factor for skin injury. The alarm can be heard in the control room.

FDAAug 17, 2006AL, AZ, AR +36 more• Datex Ohmeda, Inc

Datex Ohmeda, Inc: GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imaging...

FDAAug 17, 2006AL, AZ, AR +36 more• Datex Ohmeda, Inc

Datex Ohmeda, Inc: GE Healthcare Innova 4100 IQ Digital Fluoroscopic Imaging...

FDAAug 17, 2006AL, AZ, AR +36 more• Datex Ohmeda, Inc

International Medsurg Connection, Inc.: Allegiance Esmark 6' x 108' Bandage, Latex Free, Sterile;...

The bandages labeled as sterile had not been sterilized prior to distribution.

FDAAug 16, 2006Nationwide• International Medsurg Connection, Inc.

GE OEC Medical Systems, Inc: GE OEC 9800 Fluoro C-Arm X-ray System, GE OEC Medical Sys...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Digital Mobile C-Arm X-ray system, GE O...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: RUS Tool Version Software

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

Stryker Biotech: Calstrux (Previously known as TCP Putty)- Absorbable Bone...

Lack of Labeling Precautions. Calstrux should not be used in combination with other products and the volume used should approximate the size of the defect. Adverse reactions have been reported with over filling the defect site or combination product usage, including localized induration, swelling, inflammation, wound drainage, infection and device migration.

FDAAug 16, 2006Nationwide• Stryker Biotech

International Medsurg Connection, Inc.: Allegiance Esmark 6' x 144' Bandage, Latex Free, Sterile;...

The bandages labeled as sterile had not been sterilized prior to distribution.

FDAAug 16, 2006Nationwide• International Medsurg Connection, Inc.

Tu-Wire Dimming Ballasts (Lutron) – shock risk (2006)

The recalled ballast is used to dim compact fluorescent lighting fixtures. The ballasts are not visible once installed. The ballasts were included with light fixtures sold under numerous brand names. Consumers should not touch these fixtures, since they could pose a shock hazard. The fixtures with these ballasts have a 120 VAC application, the fixture housing is for a 26W or 32W four-pin plug-in compact fluorescent lamp installed after July 1998. Most of the lights were sold for commercial use, though some were sold for consumer use. This recall does not involve light fixtures containing incandescent or halogen lamps or fixtures with screw-in compact fluorescent lamps or straight tube (linear) fluorescent lamps.

CPSCAug 16, 2006Nationwide• Lutron Electronics Co. Inc., of Coopersburg, Pa.