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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

631

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 9641–9660 of 10391 recalls

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6201, SIngle Channel , Volumetric Infusio...

Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.

FDAJun 21, 2007Nationwide• Baxter Healthcare Corp. Rt.

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

Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.

FDAJun 21, 2007Nationwide• Baxter Healthcare Corp. Rt.

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

A software anomaly is causing newly upgraded Colleague Triple Channel Infusion Pumps to alarm, display an error code (16:310:867:0002) and stop the infusion. This occurs during user programming with all three channels simultaneously infusing fluids. In reported cases, the pump stopped infusing and both an audible and a visual alarm notification were activated.

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FDAJun 20, 2007Nationwide• Baxter Healthcare Corp. Rt.

Cardinal Health 303 Inc DBA Alaris Products: All IV Administration Infusion Sets intended for use with...

It has been determined that with low probability, over-infusion may occur as a result of an open safety clamp fitment (a.k.a. Flo-Stop fitment) on the pumping segment, whether opened intentionally in the course of expected clinical practice, or as a result of inadvertent action. The over-infusion occurrence is dependent on the user not closing the roller clamp first, as required by clinical practi

FDAJun 18, 2007PR• Cardinal Health 303 Inc DBA Alaris Products

Globe Model J Dry Fire Sprinklers – potential failure (2007)

Fire/Burn Risk

Model J Series dry fire sprinklers come in pendent, upright, and sidewall configurations. The name "Globe," the letter "J" and the year of manufacture (1990 though 1999) are embossed on the frame of each sprinkler. These dry sprinklers were designed to be installed in areas of buildings where the sprinklers or water supply pipes may be subject to freezing, such as unheated attics, freezers and coolers, parking garages, porches and warehouses.

CPSCJun 12, 2007Nationwide• Globe Fire Sprinkler Corp., of Standish, Mich.

Thermador Ceramic Cooktops – fire hazard (2007)

Fire/Burn Risk

The cooktop has electric and induction heating elements with a black ceramic glass surface. This recall involves model numbers CIT302DS/01 and CIT362DS/01 with date codes between 8606 and 8612. The model number and date code can be found on the underside of the cooktop.

CPSCJun 7, 2007Nationwide• BSH Home Appliances Corp. of Huntington Beach, Calif.

Bayer Healthcare LLC: Ascensia Contour Blood Glucose Monitoring System ( Bayer ...

Incorrect Unit of Measure displayed : The meters report results in the wrong unit of measurement for Canadian users.

FDAJun 6, 2007Nationwide• Bayer Healthcare LLC

Cardinal Health 303 Inc DBA Alaris Products: Alaris Medical Systems IV Administration Set, Low Sorbing...

The sterility of the product may be compromised as the packaging used for the sterility barrier was not designed for the sterility process used by the firm.

FDAJun 5, 2007Nationwide• Cardinal Health 303 Inc DBA Alaris Products

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLAB Target Positioner for Leksell Headring used with...

Target Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for Leksell headrings and BrainLAB planning software resulted in a 1.25 mm shift in target area alignment during radiosurgery treatment.

FDAJun 5, 2007OH, WA• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Cardinal Health: AirLife nCPAP System Driver; a nasal continuous positive ...

Under isolated conditions, the device may experience issues with O2 Calibration, which may result in either a nuisance alarm or a delivered FiO2 of up to 5% below the specified tolerance.

FDAJun 1, 2007Nationwide• Cardinal Health

The Anspach Effort, Inc.: Anspach Single Use, Sterile Bone Cutting Burrs

The white film portion of the sterile pouch may become brittle prior to the expiry date compromising the sterility of the product.

FDAMay 18, 2007Nationwide• The Anspach Effort, Inc.

Anima-Bamboo Collection Games (HaPe) – Lead Poisoning (2007)

This recall involves Anima-Bamboo Collection Games. The games contain 38 bamboo pads, four ghosts, and one dice. The product's packaging is an orange box with the words "Anima" and "BAMBOO Collection Games" printed on each side.

CPSCMay 2, 2007Nationwide• HaPe International Ltd., of Ningbo, China

Philips Medical Systems North America Co. Phillips: Achieva MRI

Potential for gaseous helium to improperly vent, resulting in rupture of the magnet vessel and venting of helium into the MRI site.

FDAApr 30, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Gyroscan MRI

Potential for gaseous helium to improperly vent, resulting in rupture of the magnet vessel and venting of helium into the MRI site.

FDAApr 30, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Intera MRI

Potential for gaseous helium to improperly vent, resulting in rupture of the magnet vessel and venting of helium into the MRI site.

FDAApr 30, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Panorama 1.0T MRI

Potential for gaseous helium to improperly vent, resulting in rupture of the magnet vessel and venting of helium into the MRI site.

FDAApr 30, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Psi Health Solutions: Psi Bands acupressure/acustimulation wrist bands in the f...

Product was marketed before its 510(k) application cleared.

FDAApr 26, 2007Nationwide• Psi Health Solutions

Thommen Medical, AG Hauptstrasse, 87 Waldenburg Switzerland: SPI EASY Abutment. Endosseous dental implant abutment.

Laceration Risk

The undercut on the SPI EASY abutments which engages the stabilization ring of the implant is missing. Although the abutments can still be placed on the implant by the user the parts do not fulfill the quality expectations of the firm.

FDAApr 19, 2007Nationwide• Thommen Medical, AG Hauptstrasse, 87 Waldenburg Switzerland

BioHorizons Implant Systems Inc One Perimeter Park South: Biohorizons 3.0mm Overdenture Implant System, REF 30120S2...

Dental implant system is missing ball attachment system.

FDAApr 18, 2007Nationwide• BioHorizons Implant Systems Inc One Perimeter Park South

Verge TV Tilt-Mount Brackets (Logitek) – Falling Risk (2007)

The recalled tilt-mount brackets for flat panel televisions are sold under Circuit City's private label, "Verge." The two model numbers involved in this recall are VPSW103M and VPSW103M2. "Verge" and the model numbers are written on the packaging. There is no writing on the brackets. The brackets were sold individually and through an installation package.

CPSCApr 12, 2007Nationwide• Logitek (HK) International Co. Ltd., of Hong Kong