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Toshiba American Medical Systems Inc

Toshiba American Medical Systems Inc Recalls

All product recalls associated with Toshiba American Medical Systems Inc.

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Recall Summary

Total Recalls

1000

Past Year

566

Class I (Serious)

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 6541–6560 of 7756 recalls

Toshiba American Medical Systems Inc: EXCELART Vantage, Atlas, and Titan MRI Systems, MRT-1503 ...

The status display in the sequence queue window may not change from "Current" to "Done".

FDAMay 13, 2008Nationwide• Toshiba American Medical Systems Inc

Datex Ohmeda, Inc. dba GE Healthcare: Corometrics MODEL 250 Series Maternal/ Fetal Monitor, Mod...

Communication connector within monitor is defective and may cause potential loss of telemetry.

FDAMay 5, 2008Nationwide• Datex Ohmeda, Inc. dba GE Healthcare

Gambro Renal Products, Inc.: Gambro Cartridge Blood Set, 0141080XXXC, is intended for ...

Dialysis tubing sets may have occlusions restricting blood flow.

FDAMay 2, 2008

1...326 327328329 330...388

Page 328 of 388Next

Nationwide

• Gambro Renal Products, Inc.

Gambro Renal Products, Inc.: Gambro Cartridge Blood Set, 003410-510, is intended for s...

Dialysis tubing sets may have occlusions restricting blood flow.

FDAMay 2, 2008Nationwide• Gambro Renal Products, Inc.

Boston Scientific Corporation: iReview" Software (Accessory To) iLab Ultrasound Imaging ...

The firm initiated a recall of a specific iReview" Software, Ver 1.0 Kit, which was released for distribution in a non-validated format.

FDAMay 2, 2008AZ, CA, FL +3 more• Boston Scientific Corporation

Abbott Laboratories Inc.: Architect / Aeroset Clinical Chemistry Iron/Magnesium Cal...

An incorrect Magnesium calibrator 2 value (CAL 2) was provided for Clinical Chemistry Iron/Magnesium Calibrator lot number 54187M200. Use of the incorrect Magnesium CAL 2 value causes quality control and patient magnesium results to be reduced by as much as 17.24% above 0.8mEq/L (1.0 mg/dL or 0.4 mmol/L).

FDAApr 24, 2008AL, AZ, CA +36 more• Abbott Laboratories Inc.

Abbott Diabetes Care, Inc.: Abbott FreeStyle Blood Glucose Monitoring System Test Str...

Flaws in strip voltage continuity may result in frequency of an Error 3 ("Er3") message display and unreadable strips. This issue has the potential for creating a delay in generating blood glucose results and to delay diabetes management, potentially leading to either hypo or hyperglycemia and their associated complications.

FDAApr 24, 2008Nationwide• Abbott Diabetes Care, Inc.

Beco Butterfly Baby Carriers – Safety Concern (2008)

The recalled infant carriers were sold under brand name "Beco Baby Carrier Butterfly." The carriers have a black label with a green "b" logo on the left side and a butterfly on the right side. The label is sewn on the outside of the carrier. The following carrier styles are included in the recall: Mia, Pony Express, Carnival, Addison, Ethan, Sophia, Cameron, Ava and Joshua.

CPSCApr 22, 2008Nationwide• Beco Baby Carrier Inc., of Newport Beach, Calif.

Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342: OMG (Observational Mechanical Gateway) Connector - A Mode...

The recall was initiated because there is a possibility that the OMG Connector-A is incorrectly packaged with an OMG Connector-M Instruction manual.

FDAApr 22, 2008Nationwide• Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342

Biomet Microfixation, Inc.: Stella Interdental Osteotome, 4mm, 6mm and 8mm. Model num...

The working tips of the Stella Osteotomes are thicker than specification.

FDAApr 16, 2008MO, NM, TX• Biomet Microfixation, Inc.

Sybaritic, Inc: Sybaritic, NannoLight MP50. Model Numbers and Descripti...

Fire/Burn Risk

Sybaritic Inc. had an issue with the 585nm filter used with the NannoLight MP50. The filter may cause unwanted burning and should not be used for vascular lesion treatments.

FDAApr 12, 2008AR, CA, FL +2 more• Sybaritic, Inc

Abbott Laboratories: CELL-DYN Sapphire Hematology Analyzer, List number 08H00-...

Table in LIS Specification depicting the association between Record ID and Numerical Result Label is incorrect. If a record ID is used to configure the system for mapping, results will come out nonsensical.

FDAApr 11, 2008Nationwide• Abbott Laboratories

Beckman Coulter Inc: Access and Access 2 Immunoassay System

The field action was initiated after the firm confirmed reports of premature failure of the waste pump tubing in the Access and Access 2 Immunoassay Systems. Premature failure of the waste pump tubing may negatively affect precision.

FDAApr 3, 2008Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: UniCel Dxl 800 Access Immunoassay System and UniCel DxC 8...

FDAApr 3, 2008Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: SYNCHRON LXi 725 System

FDAApr 3, 2008Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: Unicel DxC 600i System and Unicel Dxl 600 Access Immunoas...

FDAApr 3, 2008Nationwide• Beckman Coulter Inc

Youth Hooded Sweatshirts – Strangulation Risk (2008)

This recall involves the Youth Hooded Sweatshirt (item # 11037Y-39) and the Youth Insulated Bomber with Hood (item # 1113Y-39). The item number is found in a label located underneath the care label. The sweatshirts have a camouflage design and "Photoflauge™" is printed on them.

CPSCApr 2, 2008Nationwide• Brents-Riordan Inc. LLC, of Shreveport, La.

Celsus Laboratories Inc: Celsus Laboratories Heparin Lithium Lyophilized; Lithium ...

Contamination: The firm learned that up to 2.2% oversulfated chondroitin was found in a batch of crude heparin they received from their supplier.

FDAMar 31, 2008IN, NE, NJ +2 more• Celsus Laboratories Inc

Baxter Healthcare Corp. Rt.: Logix TPN Software Solution, catalog 2M8410, consists of ...

Software anomaly results in inaccurate information being printed out on the Delivery Report, even though the compounder performed the compounding correctly.

FDAMar 28, 2008AZ, MN, WI +1 more• Baxter Healthcare Corp. Rt.

Cozy Warming Polar Bears (Avon) – fire burn hazard (2008)

Fire/Burn Risk

The recalled white plush warming bear has a red hat and brown nose. It is about 17 inches long and comes with a buckwheat-filled pouch that is heated in a microwave oven and is inserted into an opening in the bear's belly. "Avon Products" is printed on a white tag sewn onto the bear.

CPSCMar 27, 2008Nationwide• Haiyan Boai Gifts Factory, of China