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Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp Recalls

All product recalls associated with Terumo Cardiovascular Systems Corp.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16161–16180 of 17592 recalls

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; Air Bubble Detection ...

The air bubble detection system may falsely continue to sound the air alarm after the user has disabled it.

FDAOct 16, 2006Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1, 4 inch diameter Rolle...

The pump may lose communication with the central control monitor, causing the monitor to display a service message "System Computer Needs Service" and to become non-operational.

FDAOct 16, 2006Nationwide• Terumo Cardiovascular Systems Corp

Philips Medical Systems North America Co. Phillips: Allura X-per FD 10/10 x-ray, and fluoroscopy

Potential for generator to lock-up. Fluoroscopy and x-ray is no longer possible, and system must be restarted to be able to continue.

1...807 808809810 811...880

Page 809 of 880Next

FDA

Oct 12, 2006

Nationwide

• Philips Medical Systems North America Co. Phillips

Conmed Corporation: ConMed DetachaTip Laparoscopic Instrument: Allis Multiple...

The grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.

FDAOct 12, 2006Nationwide• Conmed Corporation

Conmed Corporation: ConMed Laparoscopic Instrument: Meeker (Right Angle) Disp...

The company was made aware of instances where the grasper jaws broke during laparoscopic procedures. When the grasper jaws had broken they had done so at the junction of the jaw and the tube. In no instances was it reported to the company that small pieces had broken off of the grasper jaws.

FDAOct 12, 2006Nationwide• Conmed Corporation

Philips Medical Systems North America Co. Phillips: Allura Xper FD 20/10 x-ray, and fluoroscopy

Potential for generator to lock-up. Fluoroscopy and x-ray is no longer possible, and system must be restarted to be able to continue.

FDAOct 12, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Conmed Corporation: ConMed Laparoscopic Instrument: Allis Disposable Grasper,...

The grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.

FDAOct 12, 2006Nationwide• Conmed Corporation

GE OEC Medical Systems, Inc: OEC InstaTrak 3500, picture archiving and communications ...

GE Healthcare had recalled certain OEC InstaTrak 3500 Carts due to the potential for the cart to tip over when the arm of the imaging device is extended during use.

FDAOct 11, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC InstaTrak 3500, picture archiving and communications ...

GE Healthcare had recalled certain OEC InstaTrak 3500 Carts due to the potential for the cart to tip over when the arm of the imaging device is extended during use.

Class IIModerate

FDAOct 11, 2006Nationwide• GE OEC Medical Systems, Inc

BV4000 Blower/Vacs (Black & Decker) – Fire Risk (2006)

Fire/Burn Risk

This recall involves Black & Decker model BV4000 Type 1 blower/vacs. The model and type number are printed on a name plate on the right side of the unit. The blower/vacs have an orange housing and a black blower assembly.

CPSCOct 10, 2006Nationwide• Black & Decker (U.S.) Inc., of Towson, Md.

Fisher & Paykel Healthcare Ltd 15 Maurice Paykel Place Auckland New Zealand: Fisher & Paykel IW930 CosyCot Infant Radiant Warmer (wit...

This firm has received Product Complaint Reports concerning bending of the pivot plate. The elevator base of the CosyCot Infant Warmer incorporates a pivot plate which forms part of the mechanism allowing the CosyCot to raise and lower in height. A bent pivot plate generally results in the Warmer being unable to elevate properly. Other component failures may result.

FDAOct 9, 2006Nationwide• Fisher & Paykel Healthcare Ltd 15 Maurice Paykel Place Auckland New Zealand

St Jude Medical CRMD: St. Jude Medical Identity SR Model 5172, Identity DR Mode...

St. Jude Medical has identified a low-frequency anomaly in the software used in the APS III Model 3500/3510 and Merlin PCS Model 3650 programmers that can lead to incorrect reporting of battery voltage, expected battery longevity and Elective Replacement Indicator (ERI) status.

FDAOct 6, 2006IN• St Jude Medical CRMD

St Jude Medical CRMD: St. Jude Medical APS III Programmer, used in combination ...

FDAOct 6, 2006IN• St Jude Medical CRMD

Konica Minolta Medical Imaging USA, Inc.: Konica Minolta PrintLink III Model - ID/IV, code no. 07...

The power supply of a unit located in Japan overheated and caused a smoke condition and a small amount of flame coming off the unit.

FDAOct 6, 2006Nationwide• Konica Minolta Medical Imaging USA, Inc.

St Jude Medical CRMD: St. Jude Medical Merlin PCS Programmer, used in combinati...

FDAOct 6, 2006IN• St Jude Medical CRMD

Medtronic Emergency Response Systems, Inc.: LIFEPAK EXPRESS defibrillator

Premature battery depletion due to electrical component failure

FDAOct 5, 2006IN• Medtronic Emergency Response Systems, Inc.

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

Premature battery depletion due to electrical component failure

FDAOct 5, 2006IN• Medtronic Emergency Response Systems, Inc.

Precision Medical, Inc.: Precision Medical- Easy Mate Portable Liquid Oxygen Syste...

Component assembly; The fill chuck is not assembled properly which may allow the device to come apart over time releasing its contents.

FDAOct 4, 2006Nationwide• Precision Medical, Inc.

Del Medical Systems Group: DynaRad Phantom Portable X-Ray System; Del Medical Imagin...

The x-ray tube head assembly of the Phantom Portable X-Ray System may detach from the boom arm assembly. The tube head could fall and contact the patient or operator.

FDAOct 3, 2006Nationwide• Del Medical Systems Group

Philips Medical Systems (Cleveland) Inc: Brilliance CT System, Big Bore Configuration, Model #7282...

Two conditions have been identified with the Philips Medical System Brilliance Bore ,version 2.2.1 Tumor Localization, that may lead the user to misinterpret the displayed data.

FDAOct 2, 2006Nationwide• Philips Medical Systems (Cleveland) Inc