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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

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 10561–10580 of 10937 recalls

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Roller Pump, 115V; Model 800...

Roller Pump: Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.

FDAJul 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Fisher Diagnostic, A Company of Fisher Scientific LLC: Pacific Hemostasis D-Dimer Assay Kit, Fisher Diagnostics ...

Defective reagent may cause in vitro diagnostic test kit to yield false positive test results in clinical samples.

FDAJul 1, 2004Nationwide• Fisher Diagnostic, A Company of Fisher Scientific LLC

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Roller Pump, 1040V; Model 80...

Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.

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FDAJul 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Varian Medical Systems Inc: medical device and software systems

a malfunction in the software of the VARiS versions 6.2.27 and 6.2.35 which is used to set up radiation therapy devices which will reset parameters to null for future treatments if a patient receives treatment on a non-varian machine and a varian machine and a non-varian field is loaded in the treatment session.

FDAJun 24, 2004Nationwide• Varian Medical Systems Inc

Rock 'N Roller Baby Stroller (Dorel Juvenile Group) – Seat Detachment Risk (2004)

The COSCO® "Rock 'N Roller" strollers involved have seats that can be removed from the stroller frame. The detached seat can function as a bassinet or be repositioned on the stroller frame facing front or back. The stroller has a dark blue or green metal frame with four wheels on the front and two wheels on the back. The side folding area of the frame has a white plastic cover that is labeled "Rock 'N Roller by Geoby COSCO®." There is a label on the back of the frame containing one of the following model numbers: "01-654, 01-622, 01-624, 01-646 or 01-656." The seat cover is usually a dark blue or green printed fabric with "COSCO® A Dorel Company" printed on the footrest.

CPSCJun 23, 2004Nationwide• Dorel Juvenile Group USA, of Columbus, Ind.

Wheelbarrows (Ames) – Wheel Assembly Defect (2004)

Laceration Risk

The wheel assemblies on these wheelbarrows have a black plastic rim and have an approximately 14-inch diameter wheel. They have red, green, or orange tubs or trays made of steel or plastic and were sold under the brand names "Easy Roller," "Homeowner," "Mustang," or "Thoroughbred." The brand name was printed on the label attached to the tray at the time of purchase. Wheelbarrows with metal wheel assemblies are not part of this recall. No "True Temper" or "Jackson" wheelbarrow is part of this recall. In addition to the free replacement wheel assembly and free gardening tool incentive, the company is conducting the recall campaign with new measures to reach home gardeners who are the primary users of these recalled wheelbarrows. These new measures include placing ads in gardening publications, providing recall information to editors and webmasters of specialty gardening magazines and websites, and providing new point-of-sale posters to retailers.

CPSCJun 23, 2004Nationwide• O. Ames, a predecessor company of Ames True Temper Inc., of Camp Hill, Pa.

Toshiba American Med Sys Inc: Digital Radiography System, model DFP-8000D

Defect in the mirroring unit.

FDAJun 18, 2004Nationwide• Toshiba American Med Sys Inc

Rita Medical Systems: Dispersive Electrodes packaged in an 8x10 plastic container.

Inaccurate temperature readings may be displayed by the device, actual temperature could be 2.5-3 degrees C higher than displayed.

FDAJun 16, 2004Nationwide• Rita Medical Systems

Grocery Frozen Food Case Heaters (Electro-Heat) – Electrical Risk (2004)

The recalled defrost heater was used in Tyler's "wide island" frozen food end cap cases in grocery stores. The recalled defrost heaters (which are not visible to consumers) are Electro-Heat Defrost Heater Model 51957100. The Tyler wide island frozen food end cap cases with the recalled heaters are models NCE, NFE, NGE, NCGE, NFJEA, NCJEA, NCJGEA and NFJGEA. The model and serial number is located on the data plate, which is on the front inner panel of the case.

CPSCJun 16, 2004Nationwide• Electro-Heat Inc., of Allegan, Mich.

Cranbrook Bicycles (Huffy) – Potential Structural Failure (2004)

The recall involves single-speed "Cranbrook" bicycles with 26-inch wheels. The bicycles were sold in both men's (model 56462) and ladies' (model 56472) style frames. The name "Cranbrook" is printed on the frame of the bicycle. Serial numbers included in the recall range from SNHHE04C52556 to SNHHE04C64557. Serial numbers and model numbers are located on the bottom bracket of the frame, where the crank is attached to the bicycle.

CPSCJun 16, 2004Nationwide• Huffy Bicycle Company, of Springboro, Ohio

Reedy Quasar Pro Battery Charger (Associated Electrics) – Charging Malfunction (2004)

The recalled #611 Quasar Pro Chargers were manufactured from February 2002 through February 2004. The gray charger box has words "Quasar Pro" printed in yellow on the front and shows a display of "QUASAR PRO VERSION 1.0" when first turned on. The recalled chargers either have no barcode label on the underside or a barcode label with the numbers "611" or "611A".

CPSCJun 15, 2004Nationwide• Associated Electrics Inc., of Costa Mesa, Calif.

Fobus GLT Gun Holsters (First Samco) – Design Malfunction (2004)

The gun holsters are designed to hold a Series 17 and Series 19 Glock handgun fitted with a laser-sight light. "GL 2*EMZ" is engraved in the top of the gun holster and "FOBUS" and "MADE IN ISRAEL" is printed on the back of the gun holster. This recall involves two early versions of the Fobus GLT gun holsters, one with a plastic retention strap less than one inch wide and one with a leather retention strap less than one inch wide. The new design includes a strap that is more than one inch wide, with a plastic tip too wide to be caught inside the trigger guard.

CPSCJun 9, 2004Nationwide• First Samco, Inc., through its Fobus USA Holster Division, of Southampton, Pa.

Philips Medical Systems Sales & Service Region No. America: ViewForum Review Station Part Numbers: 9896 507 71830, ...

When reviewing images in the module before sending them to PACS or printer the order can be erratic and out of sequence and may cause confusion with the interpretation of the examination.

FDAJun 8, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: MultiDiagnost Eleva Part Numbers: 9896 001 41501 and 98...

When reviewing images in the module before sending them to PACS or printer the order can be erratic and out of sequence and may cause confusion with the interpretation of the examination.

FDAJun 8, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

DCS Wall Ovens (Dynamic Cooking Systems Inc., of Huntington Beach, Calif.) – burn hazard (2004)

Fire/Burn Risk

These wall ovens come in single or double oven models in three color options: stainless steel, black, or white. The Wall Oven/Single (WOS) models have these serial numbers, indicating the date of manufacture in 2003 and 2004 (the blank can be any of the letters A through L): 03_00001A to 03_00155A 04_00001A to 04_01093A The Wall Oven/Double (WOSD) models have these serial numbers (the blank can be any of the letters A through L): 04_00001A to 04_00210A

CPSCJun 8, 2004Nationwide• Dynamic Cooking Systems Inc., of Huntington Beach, Calif.

Philips Medical Systems Sales & Service Region No. America: EasyDiagnost Eleva Part Number 989605071921

When reviewing images in the module before sending them to PACS or printer the order can be erratic and out of sequence and may cause confusion with the interpretation of the examination.

FDAJun 8, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Dade Behring Inc. Rte 896, Glasgow Business Community: Berichrom Heparin Reagent (OWLD11). The reagent is a co...

Customers have reported a high rate of instrument error flags and calibration issues when using affected reagent.

FDAJun 7, 2004AZ, CA, CO +20 more• Dade Behring Inc. Rte 896, Glasgow Business Community

Toshiba American Med Sys Inc: Magnetic Resonance Imaging System(s) Visart and Exelar...

Fire/Burn Risk

Wrong positioning may cause patient burns.

FDAJun 7, 2004Nationwide• Toshiba American Med Sys Inc

Carl Zeiss Ophthalmic Systems Inc: Surgical powered laser instrument, used for photocoagulat...

Fire/Burn Risk

The coating of laser mirrors in a defined manufacturing lot of the Visulink 532/U devices may partially tear open and loosen from the base plate. The mirror may misdirect the laser beam to an unintended target in or on the eye. Retinal bleeding and burns may result.

FDAJun 3, 2004OR• Carl Zeiss Ophthalmic Systems Inc

Lifecore Biomedical, Inc.: TefGen is an implant material which is intended to be use...

Packaged product labeled catalog #TFS30, lot number 002419 actually contained catalog #TFR60, lot number 002441and vice versa.

FDAJun 3, 2004Nationwide• Lifecore Biomedical, Inc.