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Baxter Healthcare Corp.

Baxter Healthcare Corp. Recalls

All product recalls associated with Baxter Healthcare Corp..

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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 7981–8000 of 10391 recalls

Dextrose Injection (Baxter) – Particulate Matter Risk (2013)

Presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fibers, adhesive-like mixture, polyacetal particles, thermally degraded PVC, black polypropylene and human hair embedded in the plastic bag

Class IHigh

FDANov 21, 2013Nationwide• Baxter Healthcare Corp.

Wild'erb Seasoning (Ohio Valley Herbal) – illegal ingredient (2013)

The firm was notified by the Ohio Department of Agriculture that Sassafras Leaves may be an illegal ingredient for their product.

Class IIILow

FDANov 20, 2013CT, IN, MD +3 more• Ohio Valley Herbal Products, Inc.

Wild'erb Herbal Tea (Ohio Valley) – illegal ingredient (2013)

The firm was notified by the Ohio Department of Agriculture that Sassafras Leaves may be an illegal ingredient for their product.

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Class IIILow

FDANov 20, 2013CT, IN, MD +3 more• Ohio Valley Herbal Products, Inc.

Mini Bike (Baja Motorsports) – fall hazard (2013)

This recall involves Baja Motorsports MB200 gas-powered mini bikes manufactured from August 2010 through August 2012. The recalled mini bikes have a black frame with a black padded seat, a gas tank and fenders that are black, red or yellow, side reflectors and a headlight. A decal with the words "Baja" and "Warrior" and the number 200 inside a circle with wings attached is on both sides of the gas tank. "Baja 200cc" is on the engine cover on the right side of the minibike. This mini bike may also be known as WR96, WR200, Baja Heat, Baja Carbon and Mini Baja. The date of manufacture is on the bottom right of the Vehicle Emissions Control Information label in the MM/YY format. The label is attached to the front side of the engine.

CPSCNov 19, 2013Nationwide• Changzhou Globe Tools Co. Ltd., of China

Nitroglycerin Injection (Baxter) – Particulate Matter Risk (2013)

Presence of Particulate Matter; particulate matter in one vial identified as silicone rubber and EPDM rubber from the vial stopper.

Class IHigh

FDANov 18, 2013Nationwide• Baxter Healthcare Corp.

eXtenZone Capsules (SS Wholesale) – Undeclared API (2013)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: FDA analysis found eXtenZone which is marketed as a dietary supplement to contain undeclared desmethyl carbondenafil and dapoxetine. Desmethyl carbondenafil is a phosphodiesterase (PDE)-5 inhibitors which is a class of drugs used to treat male erectile dysfunction, making this product an unapproved new drug. Dapoxetine is an active ingredient not approved b

Class IHigh

FDANov 18, 2013CA• SS Wholesale Inc. dba Jobbers Wholesale

Clinimix 4.25/25 Injection (Baxter) – Particulate Matter Risk (2013)

Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.

Class IHigh

FDANov 18, 2013Nationwide• Baxter Healthcare Corp.

Clinimix E 4.25/10 Injection (Baxter) – Particulate Matter Risk (2013)

Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.

Class IHigh

FDANov 18, 2013Nationwide• Baxter Healthcare Corp.

Rhino 5 Capsules (SS Wholesale) – Undeclared API (2013)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: FDA analysis found Rhino 5 which is marketed as a dietary supplement to contain undeclared desmethyl carbondenafil and dapoxetine. Desmethyl carbondenafil is a phosphodiesterase (PDE)-5 inhibitors which is a class of drugs used to treat male erectile dysfunction, making this product an unapproved new drug. Dapoxetine is an active ingredient not approved by

Class IHigh

FDANov 18, 2013CA• SS Wholesale Inc. dba Jobbers Wholesale

MaXtremeZEN Capsules (SS Wholesale) – Undeclared API (2013)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: FDA analysis found MaXtremeZEN which is marketed as a dietary supplement to contain undeclared desmethyl carbondenafil and dapoxetine. Desmethyl carbondenafil is a phosphodiesterase (PDE)-5 inhibitors which is a class of drugs used to treat male erectile dysfunction, making this product an unapproved new drug. Dapoxetine is an active ingredient not approved

Class IHigh

FDANov 18, 2013CA• SS Wholesale Inc. dba Jobbers Wholesale

Clinimix 5/15 (Baxter) – Particulate Matter (2013)

Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.

Class IHigh

FDANov 18, 2013Nationwide• Baxter Healthcare Corp.

Whisper Ride Touring Wagon (Step2) – Fall Risk (2013)

This recall involves Step2® Whisper Ride Touring Wagons. The two-seat plastic wagon is 25 inches wide by 41.25 inches long by 20 inches high with blue seats, a tan wagon base and a red canopy. The Step2 logo appears on the canopy and on the side of the wagon base.

CPSCNov 15, 2013Nationwide• The Step2® Company, LLC of Streetsboro, Ohio

Alphamine (Physique) – Unapproved Ingredient (2013)

Products contain "Aegeline" an unapproved New Dietary Ingredient.

Class IIModerate

FDANov 15, 2013Nationwide• Physique Enhancing Science

Enhanced Pre-Workout (Physique) – Unapproved Ingredient (2013)

Products contain "Aegeline" an unapproved New Dietary Ingredient.

Class IIModerate

FDANov 15, 2013Nationwide• Physique Enhancing Science

Chocolate Soft Caramel (New French Bakery) – mislabeling (2013)

Undeclared Allergen

Firm discovered that 8.4 oz. jars of Hazelnut Jam were produced on 8/15/13 and were mislabeled as La Boulange Soft Caramel. the Hazelnut jam contains hazelnuts which were undeclared on the label.

Class IHigh

FDANov 13, 2013IN• The New French Bakery

Travasol Injection (Baxter) – Sterility Risk (2013)

Lack of Assurance of Sterility; Drug product leaking from container therefore sterility cannot be assured

Class IIModerate

FDANov 12, 2013Nationwide• Baxter Healthcare Corp.

ONEBODE Flo Daily (Global Health) – antibiotic contamination (2013)

The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb.

Class IIModerate

FDANov 7, 2013AZ• Global Health Laboratories, LLC

UT-Fem Supplement (Global Health Laboratories) – Antibiotic Contamination (2013)

The finished dietary supplement product was manufactured with ingredients subsequently found to be contaminated with chloramphenicol, an antibiotic, at levels above 0.3 ppb. The supplier, Specialty Enzymes & Biotechnologies, recalled the raw materials and notified the recipients. Subsequent private laboratory testing of the finished product revealed levels of chloramphenicol above 0.3 ppb.

Class IIModerate

FDANov 7, 2013NY• Global Health Laboratories, LLC

Ryobi Battery Charger (Techtronic) - Fire Risk (2013)

Fire/Burn Risk

This recall involves Ryobi model P113 dual chemistry battery chargers designed for use with both NiCd and Li-Ion portable power tool batteries. Battery chargers included in this recall are green and grey and have "Ryobi" printed in white lettering on the front of the charger. The model number and date code can be found on the data plate located on the bottom of the charger. Model P113 chargers with year/week (YY/WW) date codes between 0731-0852, without a nine digit part number, are included in the recall.

CPSCNov 5, 2013Nationwide• Techtronic Industries (Dongguan) Co. Ltd., of China

Bam Bbang Chestnut Bread (Oh Bok Bakery) - Undeclared Wheat (2013)

"Wheat" flour was not declared on the label

Class IIModerate

FDANov 5, 2013MD• Cho & So, Inc. DBA Oh Bok Bakery