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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)

127

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 23801–23820 of 25000 recalls

Terumo Cardiovascular Systems Corp: Terumo Sarns brand Soft-Flow Aortic Cannula with flange, ...

The product is labeled as sterile, but the firm has determined that the suture flange may tear through the front of the package.

FDAOct 19, 2005CA, IN, MO• Terumo Cardiovascular Systems Corp

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

While on battery power, the system may flash a low battery warning even though the battery is adequately charged.

FDAOct 19, 2005Nationwide• Terumo Cardiovascular Systems Corp

Jumbo Pencils with Sharpeners (Target) – Potential Safety Issue (2005)

Laceration Risk

The jumbo pencil has a red eraser on the end and comes with a pencil sharpener. Pencils are either short, 8 ½ inches long and one inch wide, or long, 15 inches long and ½ inch wide. The pencils are blue, red or striped. The sharpeners are pink or blue and come in a clear plastic pouch. Model number 70505 is printed on the pouch.

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CPSCOct 18, 2005Nationwide• Target Corp., of Minneapolis, Minn.

Abbott Laboratories MPG: ARCHITECT STAT Myoglobin Calibrators; list 02K43-01; each...

Some of the kits were shipped at the incorrect shipping temperature. They were shipped ambient, but should have been shipped frozen.

FDAOct 17, 2005KY, MT, PA +2 more• Abbott Laboratories MPG

Applied Medical Resources Corp 22872 Avenida Empresa # 3 Rancho Santa: The Applied GelPort Hand Access Device consists of a GelS...

The Applied GelPort Laparoscopic Hand Access Device, Model C8004. product is being recalled due to an incorrect component. The incorrect Wound Retractor base was packaged with the kit.

FDAOct 17, 2005Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa # 3 Rancho Santa

Kelty Speedster Jogging Stroller – Safety Concern (2005)

The recalled stroller has an aluminum frame and a cloth seat, with a sun canopy. The recalled stroller has model number 20050016 and serial numbers: S1000001D0504 through S1000800D0504 and S1000001D0506 through S1000200D0506. Each stroller has a tag, located inside the child's seat compartment, which lists the model name and number. A sticker on the rear frame lists the serial number. There are two yellow handle-locking clips, one on each side of the stroller frame that secures the handle from movement.

CPSCOct 14, 2005Nationwide• Kelty Division of American Recreation Products Inc., of Boulder, Colo.

Polaris Snowmobiles – Potential Mechanical Failure (2005)

Fire/Burn Risk

The recall involves all model year 2005 900 Fusion, 900 RMK, 900 Switchback snowmobiles, and select model year 2006 600HO Fusion / RMK / Switchback, 900 Fusion / RMK / Switchback, FS Classic / Touring, and FST Classic / Touring / Switchback snowmobiles. The model and serial number (VIN) identification decal is located on the right side of the tunnel underneath the seat. See affected model table below. Model Number of Affected Snowmobiles: Model Model Number 2005 900 Fusion S05MP8DS (A)(B)(C) 2005 900 RMK S05PL8DS (A)(B)(C)(D) S05PM8DS (A)(B) S05PN8DS S05PN8DE 2005 900 Switchback S05PS8DS 2006 600 HO Fusion S06MP6FS (A)(B) S06MC6FS S06ME6FS 2006 600 HO RMK S06PK6FS (A) 2006 600 HO Switchback S06PS6FS (A) 2006 900 Fusion S06MP8DS (A)(B) 2006 900 RMK S06PL8DS (A)(B) S06PM8DS (A) S06PN8DS (A) S06PR8DS 2006 900 Switchback S06PS8DS (A) 2006 FS Classic S06PD7ES 2006 FS Touring S06PT7ES 2006 FST Classic S06PD7FS 2006 FST Touring S06PT7FS 2006 FST Switchback S06PS7FS

CPSCOct 14, 2005Nationwide• Polaris Industries Inc., of Medina, Minn.

Dakocytomation California Inc: EnVision+, an ImmunoHistoChemistry reagent. This in-vitro...

This recall has been initiated due to a formulation error in the EnVision+ visualization reagent.

FDAOct 14, 2005Nationwide• Dakocytomation California Inc

Vapotherm, Inc.: Vapotherm" Respiratory Gas Humidifier, Model 2000i, label...

A medical device firm changed the labeling of its respiratory gas humidifier by revising the protocol for higher level disinfectants to be used by healthcare practitioners.

FDAOct 13, 2005Nationwide• Vapotherm, Inc.

Spacelabs Medical Incorporated: BirthNet OB Data Management System 91861

Potential for incorrect weight to be displayed.

FDAOct 13, 2005Nationwide• Spacelabs Medical Incorporated

Philips Medical Systems North America Co. Phillips: AD6 table, modified, used with the XPER systems. The mo...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: AD6 table for use with Integris and Integris Allura x-ray...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: AD5 table for use with Integris and Integris Allura x-ray...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Toshiba American Med Sys Inc: Toshiba Excelart VANTAGE Model MRT-1503, Magnetic Resonan...

To correct a hardware problem of water leakage in the cooling system inside the ASGC, leading to the replacement of the gradient coil.

FDAOct 12, 2005Nationwide• Toshiba American Med Sys Inc

Philips Medical Systems North America Co. Phillips: AD5 table, modified, used with the XPER x-ray systems. ...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

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

Six inch roller pumps were mislabeled as 4 inch roller pumps.

FDAOct 6, 2005MI• Terumo Cardiovascular Systems Corp

Reebok Children's Fleece Set – Potential Safety Issue (2005)

Choking Hazard

Only Reebok fleece pullover/pant sets with navy blue quarter-zip zippers are being recalled. The fleece pullover/pant sets were sold in navy blue/red and navy blue/pink in sizes up to children's size 7. "Reebok" is printed across the front of the pullover. The pullovers have a hood that can be folded under the collar. Some of the recalled pullovers were sold with matching mittens. The style numbers were printed on the store tag only and end in: 1816, 2816, 3816, 1816N, 2816N, 1814, 2814, 4814, and 5814.

CPSCOct 6, 2005Nationwide• Adjmi Apparel Group, of New York, N.Y. (Adjmi is an authorized licensee of children's apparel products of Reebok, of Canton, Mass.)

75-Gallon Propane Water Heaters (A.O. Smith) – Safety Hazard (2005)

Fire/Burn Risk

The recall involves 75-gallon propane gas water heaters. The heaters have the name "A.O. Smith," "Reliance," "Apollo," "State," or "Maytag" on the side of the unit. The model number is located on the rating plate. Only units with the model numbers listed below and manufactured between January 2004 and July 2005 are included in the recall. Brand Name Model Number Reliance 675CRRS 675CRRSD S7576PE Apollo A675CQRSL A675CRRSL A675CRRSLCGAD A. O. Smith BT-80-271 FCG-75-271 PCG-75-271 Maytag HRP11275Q State GS675CRRS GS675CRRSD SBS7576PE SBS7576PED SBS7576PECGA SBS7576PECGAD If your unit has one of the model numbers listed above, locate the serial number on the rating plate to determine if it was manufactured between January 2004 and July 2005. If your unit has one of the model numbers listed above, locate the serial number on the rating plate to determine if it was manufactured between January 2004 and July 2005. The serial numbers of units manufactured between January 2004 and July 2005 are listed below. Month/Date of Manufacture Serial Number Begins With: Jan-04 MA04 or AA04 or A04 Feb-04 MB04 or AB04 of B04 Mar-04 MC04 or AC04 or C04 Apr-04 MD04 or AD04 or D04 May-04 ME04 or AE04 or E04 Jun-04 MF04 or AF04 or F04 Jul-04 G04 Aug-04 H04 Sep-04 J04 Oct-04 K04 Nov-04 L04 Dec-04 M04 Jan-05 A05 Feb-05 B05 Mar-05 C05 Apr-05 D05 May-05 E05 Jun-05 F05 Jul-05 G05

CPSCOct 6, 2005Nationwide• A.O. Smith Water Products Co., of Ashland City, Tenn.

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

An incorrect serial number was placed on one roller pump.

FDAOct 6, 2005MI• Terumo Cardiovascular Systems Corp

Advanced Medical Optics, Inc.: CeeOn EDGE Silicone Posterior Chamber IOLs (Modelsl 911A ...

A small opening (channel or tunnel) in the seal of the outer Tyvek pouch which contains the lens case, in which the sealed intraocular lens is packaged may not be adequately sealed, therefore the potentially compromised outer Tyvek pouch may not be sterile and may potentially contaminate an otherwise sterile field during surgery.

FDAOct 5, 2005Nationwide• Advanced Medical Optics, Inc.