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Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt. Recalls

All product recalls associated with Baxter Healthcare Corp. Rt..

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Recall Summary

Total Recalls

1000

Past Year

567

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 6841–6860 of 7756 recalls

Baxter Healthcare Corp. Rt.: Baxter Colleague Single Channel Volumetric Infusion Pumps...

Baxter has identified the potential for a corruption of the memory chip in the pump to occur due to linear accelerator radiation exposure. If corruption occurs, it could result in an interruption of therapy with an audible and visual alarm notification to the user.

FDADec 6, 2006PR• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Colleague Triple Channel Volumetric Infusion Pumps...

FDADec 6, 2006PR• Baxter Healthcare Corp. Rt.

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: ACS DUOSTAT Rotating Hemostatic Valve, 0.096 inch, for us...

Specific lots of the .096' and .115' Rotating Hemostatic Valves (RHV) and the Duostat .096' Rotating Hemostatic Valve (RHV) potentially have an incomplete seal in the packaging pouch

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FDADec 5, 2006Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: ACS Rotating Hemostatic Valve, 0.096 inch, for use with a...

Specific lots of the .096' and .115' Rotating Hemostatic Valves (RHV) and the Duostat .096' Rotating Hemostatic Valve (RHV) potentially have an incomplete seal in the packaging pouch

FDADec 5, 2006Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Boston Scientific Target: Boston Scientific brand iLab Ultrasound Imaging System, ...

The product fails to comply with applicable electronic product performance standard, in that the electromagnetic energy is in excess of the labeled conformance standards for radiated emissions.

FDADec 1, 2006Nationwide• Boston Scientific Target

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6200 Volumetric Infusion Pump, catalog #2...

There is the potential for non-detection of, and no alarm for, upstream occlusion for Flo-Gard Volumetric Infusion Pumps, if an occlusion occurs above a flexible chamber such as a drip chamber, Buretrol or blood filter.

FDANov 27, 2006PR• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6201 Volumetric Infusion Pump, catalog #2...

FDANov 27, 2006PR• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6300 Dual Channel Volumetric Infusion Pum...

FDANov 27, 2006PR• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pum...

FDANov 27, 2006PR• Baxter Healthcare Corp. Rt.

Abbott Laboratories MPG: ARCHITECT LH Reagent, each kit contains bottles of Anti-B...

The lots of ARCHITECT LH Reagent List 6C25-22, have the potential to generate patient specimen results that are elevated. Correlation studies have demonstrated an upward shift in slope for patient results of approximately 13% on average when compared to other currently available reagent lots and an average bias from patient specimens of 13% to 17% has been observed.

FDANov 22, 2006PR• Abbott Laboratories MPG

Bio-Rad Laboratories Inc: Bio-Rad D-10 Dual Program Calibrator Diluent, a component...

The Diluent in the D-10 Dual Program Calibrator reorder packs is defective, and can cause early calibration failure or elevated control and sample recovery results.

FDANov 17, 2006Nationwide• Bio-Rad Laboratories Inc

Beckman Coulter Inc: Expo32 ADC Software Version 1.1C, Part Number 6418337-New...

The firm has confirmed that the ratio parameter assignments (numerator and denominator) of a protocol may inadvertently change after the Parameter Selection Dialog box is accessed. This issue is limited to only protocols utilizing the Ratio parameter.

FDANov 1, 2006Nationwide• Beckman Coulter Inc

Abbott Laboratories: Abbott - CELL-DYN 1800 System with CELL-DYN 22 Calibrator...

Incorrect Results: Hemoglobin results in donor samples assayed on the CELL-DYN 1800 System vary more than expected across the range of claimed operating temperatures of 18 degrees Celcius to 30 degrees Celcius.

FDAOct 27, 2006PR• Abbott Laboratories

Beckman Coulter Inc: Access Immunoassay Systems Thyroglobulin Antibody Reagent...

Low end imprecision affecting both S0 calibrators and patient samples which can lead to inaccurate low level patient results when using the Access Thyroglobulin Antibody assay.

FDAOct 26, 2006Nationwide• Beckman Coulter Inc

Beacon Outdoor Lighting Fixtures – Injury Hazard (2006)

The pendant-style outdoor lighting fixtures were installed by municipalities and developers as subdivision and/or downtown urban streetlights. The lighting fixtures typically appear along sidewalks and smaller avenues. They are made of aluminum and sold in various colors. Some have glass covers. Recalled models include "Cambridge," "Capital," "Coal Miner," Depot," "F-10 Fitter," "F-13 Fitter," "F-21 Fitter," "F-35 Fitter," "Kings Park," "Magna," "Maritas," "Miramar," "Metropolis," "Neptune," "Pierwalk," "Radial Wave" and "Tivoli."

CPSCOct 25, 2006Nationwide• Beacon Products Inc., of Sarasota, Fla.

Beckman Coulter Inc: FC 500 MPL Flow Cytometry System with MXP Software Versio...

The ratio parameter assignments (numerator and denominator) of a protocol may inadvertently change after the Parameter Selection Dialog box is accessed. Issue limited only to protocols utilizing the Ratio parameter such as LeukoSure and DNA Cell Cycle.

FDAOct 17, 2006Nationwide• Beckman Coulter Inc

ARC Bicycle Light Batteries (Light & Motion) – Fire Risk (2006)

Fire/Burn Risk

The recalled batteries are found in Light & Motion 2004 ARC Li-Ion HID lighting systems. The lights are black with "ARC" and "LIGHT & MOTION" written in yellow letters. The recall includes only batteries with a manufacturer date code of 1003 or 1103. The date code is stamped on the bottom of the battery and "LIGHT & MOTION" is printed on the side of the battery.

CPSCOct 17, 2006Nationwide• GP Batteries International Ltd., of Singapore

Boston Scientific Target: Boston Scientific brand Renegade 18 Fiber braided microca...

Incorrect expiration date: The product's exterior box date may be labeled with a longer than actual expiration date (the pouch label is correct)

FDAOct 13, 2006Nationwide• Boston Scientific Target

BV4000 Blower/Vacs (Black & Decker) – Fire Risk (2006)

Fire/Burn Risk

This recall involves Black & Decker model BV4000 Type 1 blower/vacs. The model and type number are printed on a name plate on the right side of the unit. The blower/vacs have an orange housing and a black blower assembly.

CPSCOct 10, 2006Nationwide• Black & Decker (U.S.) Inc., of Towson, Md.

Laborie Medical Technologies: Laborie Transducer Cartridge with Luer Lock Reference: DI...

Mislabeling: Product labeled with incorrect "Use Before" date and pouch labels missing lot number. (Incorrect dates-2006/07 or 2006/08; correct Use by dates-2009/08 for Lot 36H03M005 and 2009/07 for Lot 36G20M041

FDAOct 4, 2006AR, CA, FL +5 more• Laborie Medical Technologies