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KENIL HEALTHCARE PRIVATE LIMITED

KENIL HEALTHCARE PRIVATE LIMITED Recalls

All product recalls associated with KENIL HEALTHCARE PRIVATE LIMITED.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 1481–1500 of 37661 recalls

Nature Mint Toothpaste (Kenil) – CGMP Deviation (2025)

CGMP Deviations

Class IIModerate

FDAApr 24, 2025DE, NC• KENIL HEALTHCARE PRIVATE LIMITED

CURA HONGOS Antifungal (Kenil Healthcare) - CGMP Issues (2025)

CGMP Deviations

Class IIModerate

FDAApr 24, 2025DE, NC• KENIL HEALTHCARE PRIVATE LIMITED

Novum IQ LVP Infusion System (Baxter) – Infusion Risk (2025)

There is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature or if the device is powered off with the set loaded.

High

FDAApr 24, 2025

1...73 747576 77...1884

Page 75 of 1884Next

Nationwide

• Baxter Healthcare Corporation

International LT (International) – Windshield Wiper Linkage (2025)

International Motors, LLC (International) is recalling certain 2025-2026 HV, HX, LT, MV, RH, and 2025 EMV vehicles. The linkage that connects the right-side wiper arm to the motor may separate, causing the wipers to fail.

High

NHTSAApr 24, 2025Nationwide• INTERNATIONAL

Nature Mint Toothpaste (Kenil) – CGMP Deviation (2025)

CGMP Deviations

Class IIModerate

FDAApr 24, 2025DE, NC• KENIL HEALTHCARE PRIVATE LIMITED

Rapidol Antibiotic Ointment (Kenil Healthcare) - CGMP Issues (2025)

CGMP Deviations

Class IIModerate

FDAApr 24, 2025DE, NC• KENIL HEALTHCARE PRIVATE LIMITED

DxI 9000 Access Analyzer (Beckman Coulter) – Motor Installation Error (2025)

A new motor/encoder and cable was introduced into instruments manufactured starting with serial number 300141 incorrectly. This incorrect installation is introducing error codes for the Dxl 9000 which prevents the assay from being performed and a delay in results from being generated, and may require field service to resolve the delay.

Moderate

FDAApr 23, 2025Nationwide• Beckman Coulter, Inc.

Apo B Reagent (Beckman Coulter) – Calibration Error (2025)

The product Value Assignment Sheet (VAS) is used in calibration of the device. An erroneous value was included in the VAS which has the potential to generate an incorrect APO B patient result which could exceed the total allowable error for the APO B assay (11.6%). The error results in results with a positive bias up to 42%. However, based on the mitigating factors the risk to health is considered to be negligible or limited.

Moderate

FDAApr 23, 2025Nationwide• Beckman Coulter Ireland, Inc. Lismeehan O'Callaghan'S Mills Ireland

DxI 9000 Access Analyzer (Beckman Coulter) – Software Update Error (2025)

A new software update (v1.20) is introducing error codes for the Dxl 9000 which prevents the assay from being performed and a delay in results from being generated, and may require field service to resolve the delay.

Moderate

FDAApr 23, 2025Nationwide• Beckman Coulter, Inc.