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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

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 35241–35260 of 37665 recalls

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1, 6 inch diameter Rolle...

The tube clamp mechanism on the roller pump may not open when the rotation knob is turned, making it difficult to remove and/or insert tubing.

FDAAug 1, 2005GA• Terumo Cardiovascular Systems Corp

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

The power supply may fail to function due to a defective capacitor. (Note; this device incorporates a redundant separate power supply not affected by this capacitor)

FDAAug 1, 2005Nationwide• Terumo Cardiovascular Systems Corp

Boehringer Laboratories, Inc.: Boehringer Suction Regulator Model number 3704

Condition exists that prevents complete shutoff of the valve

FDA

1...1761 176217631764 1765...1884

Page 1763 of 1884Next

Aug 1, 2005

AK, AZ, CA +12 more

• Boehringer Laboratories, Inc.

Rival Crock-Pot Slow Cookers (Holmes Group) – Safety Issue (2005)

Fire/Burn Risk

The recall includes Rival® Crock-Pot® slow cookers with model numbers 3040, 3735, 5025, 5070 and 5445. The model number is printed on the UL label located on the bottom of the base. The recalled Rival® slow cooker has a removable ceramic bowl that sits inside of a metal base. The Rival® logo is printed on the front of the unit above the control knob. The bases are round or oval shaped and were sold in various colors and designs. A date code is stamped on the side of one prong of the power plug. The first two digits represent the week of manufacture and the last two digits represent the year of manufacture. Any plug with a date code from 0199 (1st week of 1999) to 3504 (35th week of 2004) is included in this recall or the previous recall.

CPSCJul 29, 2005Nationwide• The Holmes Group, of Milford, Mass.

Boston Scientific Corp: Boston Scientific brand LeVeen Needle Electrode, 5.0/13/1...

Fire/Burn Risk

Firm has received complaints of extended ablation times, lack of roll-off and patient burns.

FDAJul 29, 2005Nationwide• Boston Scientific Corp

Pioneer Surgical Technology: Pioneer Surgical brand Quantum Spinal Rod System Locking ...

The product has a higher than normal locking torque, which may cause the saddle to malfunction or to break interoperatively.

FDAJul 29, 2005Nationwide• Pioneer Surgical Technology

Pioneer Surgical Technology: Pioneer Surgical brand Quantum Spinal Rod System Polyaxia...

Screw may be incorrectly etched as to length.

FDAJul 29, 2005Nationwide• Pioneer Surgical Technology

900 Fusion RMK Snowmobiles (Polaris) – Potential Malfunction (2005)

Fire/Burn Risk

The recall includes model year 2005 Polaris "900 Fusion," "900 RMK," and "900 Switchback" snowmobiles with model numbers: S05PL8DSD, S05PM8DS(A)(B), S05PN8DS, S05PS8DS, S05PM8DS(A)(B)(C), S05PL8DS(A)(B)(C). The snowmobile model and serial number identification decal is located on the right-front side decal of the tunnel. The serial number is permanently stamped into the tunnel and the model number is embossed on the decal.

CPSCJul 28, 2005Nationwide• Polaris Industries Inc., of Medina, Minn.

Greiner VACUETTE North America: Serum Blood Collection Tubes

Serum Blood Collection tubes found with excess of Blood Clot Accelerator (BCA) solution.

FDAJul 28, 2005Nationwide• Greiner VACUETTE North America

Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany: Bard Luminexx Endoscopic Biliary Stent and Delivery Syste...

Biliary Stents may malfunction and cause failure to expand, fracture, incomplete deployment, inaccurate positioning, migration, or lumen perforation.

FDAJul 28, 2005Nationwide• Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany

Boston Scientific Marlbourgh: Adapter for ACMI Hysteroscope Catalog Number: 55035

The Hysteroscope Adapter used with the HTA System may disassemble and result in a fluid leak.

FDAJul 28, 2005CA, DE, FL +9 more• Boston Scientific Marlbourgh

Juvenile Folding Chairs (Meco) – Safety Lock Issue (2005)

Laceration Risk

The recalled children's folding chairs have safety locks under the seat. The chairs are made of metal tubing with a vinyl padded seat and seat back. They were sold in red, blue, yellow and green colors as a part of a set consisting of a table and four chairs. Each chair is about 22 inches high, 10 inches wide, and about 11 inches deep. "Meco" or "Samsonite" is printed on the label underneath the seat bottom.

CPSCJul 27, 2005Nationwide• Meco Corp., of Greeneville, Tenn.

Philips Medical Systems North America Co. Phillips: Interis Allura BiPlane X-Ray System

1) During positioning of the Lateral Stand the rotation and/or skew movement may travel unexpectedly in opposite direction; 2) movement may be faster than normal speed; 3) the stand may not stop immediately upon release of the joystick.

FDAJul 27, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Terumo Cardiovascular Systems Corp: Terumo/Capiox Cardiovascular Kit containing the CAPIOX Di...

Small cracks in the blood chamber may allow air to enter the rotor of the device

FDAJul 26, 2005AZ, CA, IL +5 more• Terumo Cardiovascular Systems Corp

Industrial Fire Extinguishers (Kidde) – Valve Malfunction (2005)

Fire/Burn Risk

This Alert involves all Kidde 10 lb. dry chemical fire extinguishers manufactured with a black plastic Zytel® nylon valve assembly and a steel cylinder, between 1991 and 2000. These units were the subject of Kidde Service Bulletin 007 issued on July 21, 2004. These units were designed for commercial and industrial applications, and the majority of these units were placed into service in factories, plants, businesses and other commercial locations, as they require service by a qualified Fire Extinguisher Distributor or Service Organization every 6 years. Some of these units are in use in residential settings. The affected extinguishers have a steel cylinder with a welded neck ring and are between 19 to 21 inches tall, as depicted in the image below. This Alert does not apply to Kidde's smaller 2 1/2 and 5 lb. residential fire extinguishers.

CPSCJul 26, 2005Nationwide• Walter Kidde Portable Equipment Inc., of Mebane, N.C.

Boston Scientific CRM Corp: CONTAK RENEWAL 3 AVT model numbers M150 and M155; CONTAK ...

Guidant is revising its original recommendations set forth in the 06/17/05 physician letter because new information indicates that one of the original recommendations can increase the risk of a latching event, which may limit available therapy.

FDAJul 25, 2005IN• Boston Scientific CRM Corp

Boston Scientific CRM Corp: VITALITY AVT, model A135 and A155. Implantable Cardiover...

FDAJul 25, 2005IN• Boston Scientific CRM Corp

Boston Scientific CRM Corp: VENTAK PRIZM AVT model no. 1900, Atrial and Ventricular T...

FDAJul 25, 2005IN• Boston Scientific CRM Corp

Bicycle Aero Bars (VisionTech) – Potential Failure (2005)

Aero bars are handlebar extensions typically used on racing and triathlon bicycles that either clip on to the handlebars or are sold as an integrated handlebar and stem system. The aero bars allow riders to ride in an aerodynamic crouching position. The recalled aero bars are an integrated system, having a cast aluminumm centerpiece, which is attached to a handlebar, a stem and two aero bars, each approximately 15 inches long, protruding in front of the handlebar. The VisionTech logo is displayed in gold lettering against a black background on the wings of the bar. Bicycle aero bars bearing a silver and red decal on the wings with the words "Vision by Full Speed Ahead" are not included in this recall.

CPSCJul 25, 2005Nationwide• VisionTech USA, Inc., of Auburn, Wash.

Smiths Medical ASD, Inc.: Bivona brand TTS Adjustable Neck Flange Hyperflex Tracheo...

Instructions for use included in the package are for a different tracheostomy tube.

FDAJul 25, 2005Nationwide• Smiths Medical ASD, Inc.