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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 10001–10020 of 10391 recalls

Baxter Healthcare Corp. Rt.: Baxter Spinal Anesthesia Trays; sterile, single use only ...

The anesthesia trays contain BD 25G Spinal Needles which which have leakage at the plastic hub of the needle.

FDAMar 28, 2005Nationwide• Baxter Healthcare Corp. Rt.

Chad Therapeutics Inc: Sequoia Oxymatic electronic oxygen conservers. Models OM-...

"Shot size" below manufacturing specifications. Risk of less than the specified quantity of oxygen delivered per pulse.

FDAMar 25, 2005Nationwide• Chad Therapeutics Inc

Abbott Health Products, Inc.: IMx total B-hCG Reagent is composed of one bottle of Coat...

Abbott Diagnostics is investigating a recent increase in customer complaints for IMx calibration error code 157 and controls out of range when using IMx total B-hCG Reagent Lot 25459Q100. Testing has shown that protein aggregates are present in the specimen diluents of both IMx and the AxSYM Total B-hCG reagent kits. This is responsible for the calibration errors and shift in control values.

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FDAMar 24, 2005Nationwide• Abbott Health Products, Inc.

Abbott Health Products, Inc.: AxSYM total B-hCG Reagent is composed of one bottle of Co...

Abbott Diagnostics is investigation a recent increase in customer complaints for AxSYM calibration error code 1048 and controls out of range when using AxSYM Total B-hCG reagent lots. Testing has shown that protein aggregates are present in the specimen diluents of both IMx and the AxSYM Total B-hCG reagent kits. This is responsible for the calibration errors and shift in control values.

FDAMar 24, 2005Nationwide• Abbott Health Products, Inc.

Abbott Health Products, Inc. Hwy 2 Km 58.0 Cruze Davila: In vitro Test TDx/TDxFLx Cyclosporine Monoclonal Whole B...

Patient results reported using calibrators made from new primary material may be falsely decreased by 5-8% compared to results using calibrators made from the previous primary material. An Important Product Information Letter with technical information regarding the Whole Blood Calibrators and Controls, implementing new internal reference standards was issued.

FDAMar 23, 2005Nationwide• Abbott Health Products, Inc. Hwy 2 Km 58.0 Cruze Davila

Baxter Healthcare Corp. Rt.: Buretrol Solution Sets, a sterile fluid pathway of variou...

The Buretrol solution sets are currently labeled as acceptable for use with the Colleague Volumertric Pump, but there is a potential for a non-detection of an upstream occlusion under certain conditions.

FDAMar 17, 2005Nationwide• Baxter Healthcare Corp. Rt.

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

The pumps may experience inadvertent power off, external communications port failures and electronic pump failure codes 402, 403, 533, 535, 599, 810:04 and 810:11.

FDAMar 15, 2005Nationwide• Baxter Healthcare Corp. Rt.

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

The pumps may experience inadvertent power off, external communications port failures and electronic pump failure codes 402, 403, 533, 535, 599, 810:04 and 810:11.

FDAMar 15, 2005Nationwide• Baxter Healthcare Corp. Rt.

ProBlend Blender (Black & Decker) – Malfunction Risk (2005)

The recall includes Black & Decker® brand ProBlend® models BL5000, BL5900 and BL6000. The recalled ProBlend® products are 5-speed, 550-watt blenders with 48-ounce marked glass jars. Each model has a die-cast, brushed stainless steel base bearing the name "Black & Decker." The model number is located on the bottom of the product.

CPSCMar 11, 2005Nationwide• Elec-Tech International Co. Ltd., of China

HID Light Fixtures (Lithonia) – Cord Safety (2005)

These are indoor HID light fixtures with acrylic reflectors and cords. They are generally used in locations such as retail spaces, light manufacturing areas, warehouse spaces, and gymnasiums. Only certain models of specific wattage lights are included in the recall. Recalled fixtures have a date of manufacture from June 3, 1999 through May 31, 2002. Check the Lithonia Web site for a list of the specific model and wattage combinations included.

CPSCMar 11, 2005Nationwide• Lithonia Lighting, of Conyers, Ga.

Baxter Healthcare Corp. Rt.: Clinician Workstation Software, product code 2M5042

The medication administration results displayed in the 'View Results' link may be inaccurate.

FDAMar 10, 2005CA, MA, MO +1 more• Baxter Healthcare Corp. Rt.

HID Light Fixtures (Lithonia) – Safety Concern (2005)

These are indoor HID light fixtures with acrylic lenses and/or reflectors. They are generally used in locations such as retail spaces, light manufacturing areas, warehouses and gymnasiums. Only certain models of specific wattage lights are included in the recall. Check the Lithonia Web site for a list of the specific model and wattage combinations included. All recalled fixtures were manufactured in Crawfordsville, Ind., and have a date of manufacture from April 2002 through October 2003. The models, wattages, city and date of manufacture, and the name "Lithonia," can be found on a label attached to the ballast housing. This recall also includes certain replacement ballast kits within the above dates of manufacture.

CPSCMar 8, 2005Nationwide• Lithonia Lighting of Conyers, Ga.

Abbott Health Products, Inc.: IMx HAVAB Controls In Vitro Test

Abbott identified through investigational studies that IMxHAVAB Controls lot 21059Q100 is generating Negative Control values outside the upper range specified in the IMxHAVAB Package Insert.

FDAMar 4, 2005Nationwide• Abbott Health Products, Inc.

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

Inadequate directions for use resulting in fluid leaks, valves sticking in the open position, and flow output restriction.

FDAMar 3, 2005Nationwide• Baxter Healthcare Corp. Rt.

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

Inadequate directions for use resulting in fluid leaks, valves sticking in the open position, and flow output restriction.

FDAMar 3, 2005Nationwide• Baxter Healthcare Corp. Rt.

Stuffed Yarn Bunny (Ocean Desert Sales) – Potential Safety Issue (2005)

Choking Hazard

The stuffed bunny is about 8 inches tall, wearing a skirt or overall shorts in various colors, including purple, turquoise and pink. The skirt and overall shorts are decorated with heart and flower buttons, and there is a bow tie at the neck in checked pattern colors including green and pink. The eyes are round black beads. A hang tag attached to the stuffed bunny reads in part, "OCEAN DESERT SALES 5400 TULIP STREET, PHILADELPHIA, PA 19124 ITEM NO.: EST-220 MADE IN CHINA UPC CODE: 0 15381 14220 1."

CPSCMar 2, 2005Nationwide• Ocean Desert Sales Inc., of Philadelphia, Pa.

Baxter Healthcare Corp. Rt.: Configuration Transfer Cable; an accessory for the Collea...

The Configuration Tranfer Cable for the Colleague Infusion Pumps has incorrect thumb screws on it., not allowing firm connections of the cable to the pump to transfer data to the biomedical engineer's diagnostic device.

FDAMar 2, 2005Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter ClearLink Intravenous (IV) Solution Sets and Exte...

Possible occlusion of the Clearlink injection site valve due to inadequate silicone lubrication of the slit in the upper seal of the valve.

FDAFeb 28, 2005Nationwide• Baxter Healthcare Corp. Rt.

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

Swelling of the sealed lead-acid batteries in the infusion pump can cause internal pump damage, and excessive battery discharge can damage the batteries if the pump is left on battery power for an extended period of time after teh Battery Depleted alarm occurs.

FDAFeb 25, 2005Nationwide• Baxter Healthcare Corp. Rt.

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

FDAFeb 25, 2005Nationwide• Baxter Healthcare Corp. Rt.