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Baxter Healthcare Corporation

Baxter Healthcare Corporation Recalls

All product recalls associated with Baxter Healthcare Corporation.

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Recall Summary

Total Recalls

1000

Past Year

590

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 2481–2500 of 10391 recalls

Baxter CLEARLINK System (Baxter) – Solution Set Leaks (2022)

Firm noted an increase in customer reports of leaks.

FDAAug 9, 2022Nationwide• Baxter Healthcare Corporation

Highland Ridge SilverStar XLT (Highland Ridge) – Structural Issue (2022)

Highland Ridge RV (Highland Ridge) is recalling certain 2022 Mesa Ridge, Mesa Ridge S-lite, Mesa Ridge XLT, Olympia, Olympia Lite, Olympia Sport, Open Range, Open Range Light, Open Range Roamer, Range Lite, Range Lite Air, Silverstar, Silverstar S-lite, and Silverstar XLT trailers. The electric retractable awning has a welded seam on the fabric that may separate, potentially allowing the awning to drop beyond normal operation.

NHTSAAug 4, 2022Nationwide• HIGHLAND RIDGE

Ditch Witch VT14 (Ditch Witch) – Certification Label (2022)

Charles Machine Works, Inc. is recalling certain 2020-2022 Ditch Witch VT24, VT12, VT14, and 2022 VT14MV trailers. The vehicle certification label does not have the correct Gross Axle Weight Rating (GAWR) listed. As such, these vehicles fail to conform to Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and rims - other than passenger cars."

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NHTSAAug 4, 2022Nationwide• DITCH WITCH

Acetaminophen Injection (Baxter Healthcare) – Temperature Abuse (2022)

Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled room temperature environment.

Class IIModerate

FDAAug 4, 2022Nationwide• Baxter Healthcare Corporation

Stryker EVOLVE Proline Stem (Wright) – Label Mismatch (2022)

The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem 9.5mm +4 contains a size 7.5mm +2 stem.

FDAAug 3, 2022Nationwide• Wright Medical Technology, Inc.

Zynrelef (Heron Therapeutics) – Defective Syringe (2022)

Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe packaged in one lot of Zynrelef 400 mg/12 mg kit

Class IIILow

FDAAug 2, 2022Nationwide• HERON THERAPEUTICS, INC.

Creamy Creations Light Ice Cream (H-E-B) – undeclared wheat (2022)

Undeclared Gluten

Undeclared wheat

Class IIModerate

FDAAug 1, 2022TX• H-E-B Grocery Company, LP DBA HEB Milk & Culture Plant #80645

Evaporator Coil Drain Pans (Daikin) – expanded product recall (2022)

Fire/Burn Risk

This recall expands the scope of a previous recall that involved certain evaporator coil drain pans installed with condensing gas furnaces in an up-flow coil configuration. The recall now also includes those drain pans installed with certain configurations of competitor branded (not Goodman, Daikin or Amana-branded) non-condensing residential gas furnaces in a vertical, or "up-flow," coil configuration, as shown in the table below: Type Coil Configuration Affected Furnace Brands Affected Coil Serial Numbers Dates Sold Condensing furnace system Up-Flow (Coil above Furnace) All Prefixes ranging from 1901 through 2101 Jan. 2019 through Nov. 2021 Non-condensing furnace system (Certain configurations) Up-Flow (Coil above Furnace) Any "competitor" brand (excludes Goodman, Daikin or Amana branded furnaces) Prefixes ranging from 1901 through 2101 Jan. 2019 through Nov. 2021 NOTE: Furnace systems that were repaired with a new evaporator coil drain pan between January 2019 and November 2021, with the serial number range listed above, are also included in this recall. Whether a non-condensing furnace system falls within the scope of the expanded recall depends on the location of the burners, which, if unknown, can be verified through DCT's model verification tool at: https://www.recallrtr.com/drainpan. Affected units can be identified through serial numbers found on the evaporator coil or the case, which sits atop the vertically installed furnace. The furnace brand and model number can be found on the furnace on the "Energy Guide" label. Consumers can refer to the instructions on DCT's model verification tool at: https://www.recallrtr.com/drainpan. The model number of the outdoor condenser may also be required and can be found on a label attached to the product.

CPSCJul 28, 2022Nationwide• Daikin Comfort Technologies Manufacturing, L.P. (formerly Goodman Manufacturing Company, L.P.) of Houston, Texas

Stryker Swanson Finger Joint Implant (Wright Medical) – Incorrect Sizing (2022)

An incorrect sizing label was applied to the carton packaging.

FDAJul 27, 2022Nationwide• Wright Medical Technology, Inc.

Orca Foam Cube (Gelita Medical) – Endotoxin Levels (2022)

In routine bioburden testing, higher than acceptable levels of Endotoxins were observed.

FDAJul 27, 2022Nationwide• GELITA MEDICAL GMBH Uferstr. 7 Eberbach Germany

Azacitidine Injection (Amerisource) – Subpotent Drug (2022)

Subpotent Drug

Class IIILow

FDAJul 27, 2022Nationwide• Amerisource Health Services LLC

NARMD Medical Depot Scissors (Stradis) – Sterile Barrier (2022)

The sterile barrier may be compromised.

FDAJul 25, 2022Nationwide• Stradis Medical, LLC dba Stradis Healthcare

NARMD Medical Depot Forceps (Stradis) – Sterile Barrier (2022)

The sterile barrier may be compromised.

FDAJul 25, 2022Nationwide• Stradis Medical, LLC dba Stradis Healthcare

Baxter DISCPAC Syringe Caps (Baxter) – Packaging Sterility (2022)

There is a potential of the packaging not maintaining a sterile barrier for the tip caps.

FDAJul 22, 2022Nationwide• Baxter Healthcare Corporation

Cheetah 7235SNFSX Trailer (Cheetah) – Twist Lock Handles (2022)

Cheetah Chassis Corporation (Cheetah) is recalling certain 2023 7400GNFF0, 7235SNFSX, and 8400GNFF0 trailers. The Tandemloc twist lock handles may separate from the trailer and fall to the ground.

NHTSAJul 21, 2022Nationwide• CHEETAH

Dimension Vista LOCI CA 15-3 (Siemens) – Sample Bias Risk (2022)

Negative bias with patient samples. The mean patient sample bias range from -26% to -33%,potential risk of delay in appropriate treatment and management decisions.

FDAJul 18, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Centricity Universal Viewer (GE Healthcare) – Measurement Inaccuracy (2022)

Inaccurate Distance and Area measurements with use of Global Stack viewport.

FDAJul 15, 2022AZ, AR, CA +37 more• GE Healthcare, LLC

Exacta-Mix 2400 System (Baxter) – Valve Leakage Potential (2022)

There is a potential for leaking valves on ports 1 to 4 in certain lots of valve sets.

FDAJul 14, 2022Nationwide• Baxter Healthcare Corporation

HXBL Viral Transport Container (Haimen Shengbang) – Distribution Guidance Violation (2022)

Distributed VTM outside of VTM Guidance and without clearance.

FDAJul 12, 2022Nationwide• Haimen Shengbang Laboratory Equipment Co. Ltd. D, Sanhe No. 50 Xue Qian Road; Sanhezhen Haimen Nantong China

Surpria 64 Software (FUJIFILM) – Scanning Error Risk (2022)

Error 00003050 or 00003052 may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation

FDAJul 12, 2022Nationwide• FUJIFILM Healthcare Americas Corporation