Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Brands International Corporation

Brands International Corporation Recalls

All product recalls associated with Brands International Corporation.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

135

Class I (Serious)

159

Most Recent

Dec 2025

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 141–160 of 1146 recalls

Diabetics Foot Cream (Brands International) – Inadequate Testing (2024)

CGMP Deviations: lack of adequate release testing.

Class IIModerate

FDANov 13, 2024Nationwide• Brands International Corporation

2025 International HX (International) – Axle Lubrication Issue (2024)

International Motors, LLC (International) is recalling certain 2024-2025 HX vehicles. An insufficient amount of lubricant in the front steer drive (FSD) axle hubs may result in damage to the wheel bearings.

NHTSANov 4, 2024Nationwide• INTERNATIONAL

2025 International HV (International) – software communication issue (2024)

International Motors, LLC (International) is recalling certain 2021-2024 Lonestar, 2021-2025 RH, HV, MV, LT, HX, and 2022 PROSTAR vehicles, equipped with Bendix EC80 Advanced Electronic Control Units (ECU). Electrical noise and low signal to the power line carrier may cause the ECU to incorrectly process commands or stop working.

1...6 789 10...58

Page 8 of 58Next

NHTSAOct 31, 2024Nationwide• INTERNATIONAL

Chlorpheniramine Tablets (BLI) – Stability Assay Issue (2024)

Superpotent Drug: Stability failure for assay at 6 months test time-point.

Class IIModerate

FDAOct 21, 2024MO, OH• BLI International, Inc.

DRG:HYBRiD-XL Insulin (DRG International) – Recalibration Failure (2024)

The user of the assay may either face a failure message during re-calibration of the Hybrid.XL instrument using the re-calibration R1 and R2 of the device or find controls out of specification (failed Control High) which causes a delay in results.

FDAOct 7, 2024Nationwide• DRG International, Inc.

International HX (INTERNATIONAL) – Fuel Pump Delivery Problem (2024)

Navistar, Inc. (Navistar) is recalling certain 2025 International HX and International LT vehicles equipped with Cummins X15 diesel engines. The fuel pump barrels may fracture and cause a fuel leak, resulting in an engine stall.

NHTSAOct 1, 2024Nationwide• INTERNATIONAL

International CV (INTERNATIONAL) – Air Bag Module Activation Issue (2024)

Navistar, Inc. (Navistar) is recalling certain 2025 International CV vehicles. The air bag module may not have been activated during installation.

NHTSAOct 1, 2024Nationwide• INTERNATIONAL

17-OH Progesterone ELISA Kit (DRG) – Control Range Mismatch (2024)

The High and Low Control acceptance ranges in the Certificate of Analysis (CofA) did not match the acceptance range information on the High and Low Control Component labels. Due to the defect, the device failed to provide results, which may result in a delay in obtaining test results and a remote chance of an adverse health risk.

FDASep 13, 2024AZ, CA, GA +1 more• DRG International, Inc.

AirJet HydroJet Spa Pumps (Bestway) – Fire Hazard (2024)

Fire/Burn Risk

The spa pumps could have been sold separately, or in a package with an inflatable spa liner in different colors, styles, and inflatable spa sizes. The inflatable spa liners packaged with the pumps are sold under the brand names SaluSpa, Coleman, and Hydro-Force, which are printed on the side of the liner. This recall only includes AirJet and HydroJet Spa Pump model numbers P05332, P05339, P05711, P05807, P07000, P07001, P05511, P07034, and P07572. "Bestway" and the model number are printed on the label on the side or back of the spa pump.

CPSCSep 12, 2024Nationwide• Bestway (Hong Kong) International Ltd., of China

J-Basket Napa Kimchi (JFC International) – yeast growth (2024)

High levels of Yeast growth and film on top of jarred Kimchi product.

Class IIModerate

FDAAug 1, 2024AZ, CO, FL +7 more• J F C International Inc

CustomEyes Procedure Packs (Beaver Visitec) – Syringe Recall (2024)

Data in RES.

FDAJul 26, 2024Nationwide• Beaver Visitec International, Inc.

CustomEyes Procedure Packs (Beaver Visitec) – Syringe Recall (2024)

Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI CustomEyes Procedure Packs.

FDAJul 26, 2024Nationwide• Beaver Visitec International, Inc.

Arrow Arterial Kits and Trays as follows: (1) Arrow Arte... (ARROW INTERNATIONAL Inc.) – reports have been received regarding ... (2024)

Reports have been received regarding open seals on the packaging.

FDAJul 26, 2024Nationwide• ARROW INTERNATIONAL Inc.

2025 INTERNATIONAL HX – navistar, inc (2024)

Navistar, Inc. (Navistar) is recalling certain 2025 International HV, HX, LT, MV, and RH vehicles. The tie rod assemblies may contain ball studs that have been incorrectly heat-treated, which can cause them to break, and possibly result in tie rod failure.

NHTSAJul 25, 2024Nationwide• INTERNATIONAL

Salivary Testosterone ELISA (DRG) – Invalid Controls (2024)

Invalid Controls. The Low Control is out of range; too high which causes invalid runs that would result in repeating the runs and delays for reporting results to patients.

FDAJul 5, 2024Nationwide• DRG International, Inc.

2025 International RH (International) – Tie Rod Assembly Defect (2024)

Navistar, Inc. (Navistar) is recalling certain 2025 International HV, LT, MV, and RH trucks. Tie rod assemblies may contain ball studs that may have been incorrectly heat-treated, which can cause them to break, and possibly result in tie rod failure.

NHTSAJun 20, 2024Nationwide• INTERNATIONAL

Oatmeal Body Lotion (Brands International) – Mold Contamination (2024)

Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination

Class IIModerate

FDAJun 10, 2024Nationwide• Brands International Corporation

Cinnamon Powder (Shahzada) – Elevated Lead Levels (2024)

Product contains elevated levels of lead (2,030 ppb)

Class IIModerate

FDAMay 21, 2024CT, MA, NJ +1 more• Advance Food International Inc.

Xstar Safety Slit Knife (Beaver Visitec) – Blade Configuration Error (2024)

The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down).

FDAMay 10, 2024Nationwide• Beaver Visitec International, Inc.

Ultra 8 IAB Catheter Kit (Arrow) – Health Consequence (2024)

Teleflex received reports indicating an infrequent condition that, when not identified and corrected promptly, could result in serious health consequences. The issue may manifest as: -failure of the intra-aortic balloon to completely inflate over its full length -damaged or broken central lumen in the segment contained within the balloon -helium loss or blood in the helium pathway.

FDAApr 29, 2024Nationwide• ARROW INTERNATIONAL Inc.