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Terumo Cardiovascular Systems Corporation

Terumo Cardiovascular Systems Corporation Recalls

All product recalls associated with Terumo Cardiovascular Systems 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 32761–32780 of 37665 recalls

Terumo Cardiovascular Systems Corporation: Terumo Advanced Perfusion System 1 Base, 100/120V; Model ...

The pumps may exhibit blank or distorted displays, loss of local control and/or may have local control knobs that are difficult to use.

FDAJul 18, 2008Nationwide• Terumo Cardiovascular Systems Corporation

Terumo Cardiovascular Systems Corporation: Terumo Advanced Perfusion System 1 (4 inch diameter Rolle...

Overspeed and underspeed errors, erratic pump behavior, jerky operation at low RPMs, pump instability, pump slowdowns and pump stops due to overspeed max events may occur due to a grease leak onto the motor speed encoder disk.

FDAJul 18, 2008Nationwide• Terumo Cardiovascular Systems Corporation

American Medical Systems: AMS 700 CX MS Pump IZ, Preconnect Penoscrotal, 18 cm, Ste...

The carton labeling does not match the product packaged inside. The package indicated that the device is an 18cm Preconnected MS pump while it is actually an 18cm Ultrex Preconnected MS Pump.

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FDAJul 17, 2008LA• American Medical Systems

Spacelabs Healthcare, Incorporated: Ultraview Digital Telemetry Transmitter, Model 91341-09 T...

During battery insertion there is potential for patient waveforms to move to an open receiver module or to an occupied receiver causing the intermittent inappropriate monitoring of both patients for several minutes.

FDAJul 17, 2008Nationwide• Spacelabs Healthcare, Incorporated

SpeeCo Log Splitter Engines – Fire Hazard (2008)

Fire/Burn Risk

The recall involves Honda engines (model type GCV160LA N1A) used in Split Master by SpeeCo and Huskee brand log splitters. Only engine serial numbers between 5547012 and 6880908 are included in the recall. The serial number is located below the upper shroud near the oil dipstick. The following models of log splitters are affected by the recall and are either silver/black or red/black colored. Huskee Log Splitter LS401227TS (22 Ton) LS401228NO (27 Ton) SpeeCo Split Masters LS401228SP (22 Ton) LS401227NO (22 Ton) LS401225NO (25 Ton)

CPSCJul 17, 2008Nationwide• American Honda Motor Corp., of Torrance, Calif.

Honda TRX420 Rancher ATVs – Control Loss Risk (2008)

This recall involves Model Year 2007-08 Honda TRX420 ATVs, also known as the Honda FourTrax Rancher 4X4. These are adult-size ATVs designed for use by riders age 16 and older. The recalled ATVs are available in red, black, olive, and camouflage. The Honda name and wing logo are printed on the fuel tank. The model year is printed on a label located on the frame behind the left front wheel. The model name "Rancher" is on a label at the left rear of the ATV.

CPSCJul 17, 2008Nationwide• American Honda Motor Co. Inc., of Torrance, Calif.

Silhouette TV Stands – Tip-over Risk (2008)

This recall involves "Silhouette" TV stands with black or brushed silver and black frames and three glass shelves. Models included in the recall are 403650 (brushed silver and black) and 404191 (black). Model numbers are printed on the packaging and instruction sheet.

CPSCJul 17, 2008Nationwide• King Pao Enterprise Co. Ltd., of Guangdong, China

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Harvest Needle, Medical Device Tec...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Aspiration Needle, Medical Device ...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

GE Healthcare Kuortaaneenkatu 2 Helsinki Finland: GE Healthcare, Mobile Care Server used in conjunction wit...

Issue 1 -Possible failure of CIC Pro audible alarms: Requests for telemetry defaults from Mobile Care Server could cause excessive CIC Pro memory consumption. This excessive memory consumption may lead to potential loss of audio at the CIC or a system reset or reboot. Issue 2 - Mobile Care software/Mobile Viewers don not recognize ApexPro FH Telemetry transmitter: Mobile Care server does not ac

FDAJul 16, 2008CA, IN, IA +2 more• GE Healthcare Kuortaaneenkatu 2 Helsinki Finland

Medical Device Technologies, Inc.: Angiotech, T-Lok Bone Marrow Biopsy Needle, Medical Devic...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Biopsy Needle, Medical Device Tech...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Philips Medical Systems: HeartStarMRtX Defibrillator/Monitor Models: M3535A/M3536A...

Defective internal memory cards may exhibit one or more of the following behaviors: "Device repeatedly restarts approximately every 20 seconds "Slow device start-up of approximately 15 seconds or more. During this time, the MRx displays either a blank screen or the Philips HeartStart MRx Start-up screen prior to displaying the selected mode of operation (i.e. Monitor, AED, Pacing or Manual Defib mode). "Internal Memory Failure INOP message when attempting to print an event from the Data Management screen. "When printing from the Data Management screen, a patients Event Summary prints with some clinical events missing.

FDAJul 14, 2008Nationwide• Philips Medical Systems

Theken Spine LLC: FormPutty Bone Void Filler 10cc The product is sealed i...

The patient label inside the package has an expiration date of 2008-06 when the actual expiration date is 2010-06.

FDAJul 11, 2008Nationwide• Theken Spine LLC

Polaris Snowmobiles – Rider Injury Risk (2008)

The recall involves 2008 Polaris 550 LX, Trail Touring and Trail Touring Deluxe snowmobiles. The model and serial number identification decal is located on the right side of the tunnel below the seat. The recalled model names and numbers are listed below. There is also a limited quantity of suspect parts (about 290) that were sold to consumers for service work or accessory starter installations. These parts could fit on various 2003 through 2007 models of snowmobiles and were sold from March 3, 2007 through October 22, 2007. Model Number Model Year Market Name S08ND5BS 2008 550 LX S08NT5BS 2008 Trail Touring S08NT5BE 2008 Trail Touring S08NT5BSA 2008 Trail Touring Deluxe S08NT5BSF 2008 Trail Touring Deluxe

CPSCJul 11, 2008Nationwide• Polaris Industries Inc., of Medina, Minn.

Propane Storage Tanks – Gas Leak Risk (2008)

Fire/Burn Risk

The recall includes 120-gallon to 1,000-gallon underground propane storage tanks which were previously converted from above-ground to underground storage tanks in the period of January 2005 through April 2008.

CPSCJul 11, 2008Nationwide• American Welding & Tank LLC, of Jesup, Ga.

Depuy Orthopaedics, Inc.: Depuy DELTA Xtend, Standard humeral PE Cup Dia 38/+3 STD,...

Compressed air may become trapped between the cup and the stem, preventing the tapered walls from engaging and causing the cup to feel unstable.

FDAJul 10, 2008Nationwide• Depuy Orthopaedics, Inc.

Honda Lawn Mowers – Laceration Hazard (2008)

Laceration Risk

This recall involves HRX walk-behind lawn mowers with model numbers HRX217(K)2HXA and HRX217(K)2HMA. The model and serial number are printed on a label located on the upper rear of the mower deck. Serial numbers included in the recall are MAGA-1500001 through 1520532. The recalled lawn mowers are red with "HONDA" written on the bag.

CPSCJul 10, 2008Nationwide• American Honda Motor Corp., of Torrance, Calif.

Beckman Coulter Inc: Synchron Acetaminophen (ACTM) Reagent, Part Number 47216...

This recall was initiated after Beckman Coulter verified through testing that Acetaminophen reagents (lots #M702524 & M703276) manufactured with contaminated heparin has shown a negative bias in performance between the assay made with contaminated and uncontaminated heparin.

FDAJul 10, 2008Nationwide• Beckman Coulter Inc

Merit Medical Systems, Inc.: 10ml Control Syringe, REF/CAT No.: CCX011 Version A, Ster...

Control Syringes may be non-sterile due to holes in the packaging.

FDAJul 9, 2008CA, FL, GA +11 more• Merit Medical Systems, Inc.