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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)

145

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 35661–35680 of 37661 recalls

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

System 1 power supply may electrically short to the main console, disrupting normal system operation by causing unexpected re-setting or shutdown of pumps and modules, false alarms and/or overheating and failure of the central control monitor.

FDAFeb 1, 2005Nationwide• Terumo Cardiovascular Systems Corp

The Spineology Group: Fill Tube,diverted, Catalog # 300-1002, is used for the ...

Three malfunctions, due to jamming of bone material in the fill tube occurred, which allowed the fill tube to advance more deeply than intended into the surgical site. Fill tubes are used in delivery of bone graft materials.

FDAJan 28, 2005AZ, AR, CA +8 more• The Spineology Group

The Spineology Group: Platen, Catalog # 301-124, is a mechanism used to lock or...

1...1782 178317841785 1786...1884

Page 1784 of 1884Next

FDAJan 28, 2005AZ, AR, CA +8 more• The Spineology Group

Greer Laboratories Inc: Sterile Empty Vials for Allergenic Extracts, 100ml size

Product may not be sterile.

FDAJan 28, 2005AZ, CA, FL +14 more• Greer Laboratories Inc

Medtronic Surgical Navigation Technologies, Inc: Stealth Station Cranial Application v.4.5

The Stealth Station Cranial Application Version 4.5 contains a software anomaly, which may present a hazard to the patient.

FDAJan 28, 2005AL, AZ, AR +20 more• Medtronic Surgical Navigation Technologies, Inc

The Spineology Group: Fill Tube,straight, Catalog # 300-1001, is used for the ...

FDAJan 28, 2005AZ, AR, CA +8 more• The Spineology Group

Guidant Corporation Advanced CardiovascularSystem: Voyager RX Coronary Dilatation Catheter

Leak at guide wire exit notch could introduce air into the artery.

FDAJan 27, 2005IN• Guidant Corporation Advanced CardiovascularSystem

AMF Support Surfaces Inc: Cool/Heat Versatility Main Controller Unit with 7-pin por...

Operator misconnected device power cords causing failure of the device.

FDAJan 27, 2005IN, MD, ND• AMF Support Surfaces Inc

GE OEC Medical Systems, Inc: InstaTrak 3500 Plus system with cranial application (aid ...

Tracking inaccuracy of 5-10 mm may result when the shunt guide accessory is used with version 5.1 software.

FDAJan 26, 2005AL, AK, AZ +21 more• GE OEC Medical Systems, Inc

Jumpking Trampolines (Jumpking Inc.) – Potential Injury Risk (2005)

Laceration Risk

The recall includes 14-foot and 15-foot Jumpking trampolines sold separately and with FunRing enclosures. The brand name "Jumpking, Inc." is written on a warning label wrapped around a leg of the trampoline. The eight legs of these trampolines fit into perpendicular sockets welded to the top rails. Trampolines with weldless sockets that fit over the connecting top rail pieces are not included in this recall. The FunRing enclosures have an arched design where the vertical poles are connected by arches at the top. Some enclosures were sold separately from the trampolines. Later units, that include the rubber sleeves that fit around the mounting brackets, are not included in the recall.

CPSCJan 25, 2005Nationwide• Jumpking Inc.® of Mesquite, Texas

Stryker Howmedica Osteonics Corp.: Short Barrel Sideplate, Omega + 140 degrees, 4 slots; The...

Stryker Orthopaedics became aware that the packaging labeled as catalog number 3362-0-040; lot code E00985, 140 x 4 slot may contain a 5 hole slot.

FDAJan 25, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Bio Rad Laboratories, Inc.: Bio-Rad Pathfinder RSV Test Kit. Top of kit labeled PATH...

New instructions to recommend against using samples with visibly high level of blood.

FDAJan 25, 2005Nationwide• Bio Rad Laboratories, Inc.

Chamois Blankets (Pottery Barn Kids) – Material Safety (2005)

This recall involves children's chamois blankets made of 100% polyester. The blankets were sold in yellow, pink, blue and green, and the reverse side of all the blankets are white. Decorative yarn in a coordinating color is stitched around the blanket's edge. The blanket measures 30 inches wide by 40 inches long and are labeled for stroller use. A label on the blanket reads "pottery barn kids" and "Made in Korea."

CPSCJan 24, 2005Nationwide• Pottery Barn Kids, of San Francisco, Calif.

Kinetic Concepts, Inc: RotoProne powered patient rotation bed, part #209500, dis...

To correct software issues in software versions 1.3 and 1.5 and to upgrade hatch latch handles to a more ergonomic design.

FDAJan 24, 2005Nationwide• Kinetic Concepts, Inc

Integra Neuro Sciences: LICOX Complete Brain IMC Probe Kit, Model IM3.ST C

LICOX Model C8.B temperature probes manufactured by GMS mbH, an Integra company, may exhibit progen (endotoxin) levels above the FDA limit of 2.15 endotoxin units per device. Elevated endotoxin levels may result in an increased patient risk of fever.

FDAJan 21, 2005CA, CO, DE +21 more• Integra Neuro Sciences

Integra Neuro Sciences: LICOX temperature probe, Model C8.B

FDAJan 21, 2005CA, CO, DE +21 more• Integra Neuro Sciences

Baxter Healthcare Corp. Rt.: Baxter Posiflow Access Device for IV Access; product code...

Product older than three years may not operate as intended.

FDAJan 20, 2005Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Extension Sets with Posiflow Access Device for IV ...

Product older than three years may not operate as intended.

FDAJan 20, 2005Nationwide• Baxter Healthcare Corp. Rt.

Fun Years Music Big Drum Set (Kids Station) – Potential Injury (2005)

Choking Hazard

The recalled music set includes a yellow and green drum with a clear plastic lid and a red one-piece carrying strap that doubles as a storage and carrying case for additional instruments. The drum measures 12 inches in diameter and about 7.5 inches in height. The instruments stored in the drum include: purple drumsticks, yellow and red dumb-bell-shaped maracas, purple wrist bells, an orange recorder, a yellow harmonica, a red-rimmed tambourine and a yellow whistle. Only this musical set is part of this recall. A similar drum set sold at Toys "R" Us with a two-piece strap and different musical toys is manufactured by a different company and is not being recalled.

CPSCJan 19, 2005Nationwide• Kids Station Inc., of Miami, Fla., for Toys "R" Us, of Wayne, N.J.

North Coast Medi-Tek Inc: SourceOne Healthcare Technologies brand, Ultrasound Tray,...

Outside box labeling, containing 10 trays, incorrectly identified the product as ultrasound trays. Product is Breast Biopsy trays, Cat. 255826R2. Individual tray package labeling correctly identifies the product as Breast Biopsy tray.

FDAJan 18, 2005OH• North Coast Medi-Tek Inc