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ARG Laboratories, Inc.

ARG Laboratories, Inc. Recalls

All product recalls associated with ARG Laboratories, Inc..

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Recall Summary

Total Recalls

1000

Past Year

567

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 881–900 of 7756 recalls

Pain Wizard (ARG Laboratories) – Active Ingredient Violation (2024)

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Class IIModerate

FDAApr 17, 2024Nationwide• ARG Laboratories, Inc.

Golden Tiger Pain Cream (ARG Laboratories) – Active Ingredient Violation (2024)

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Class IIModerate

FDAApr 17, 2024Nationwide• ARG Laboratories, Inc.

Aloe Gator Sunscreen (ARG Laboratories) – Ingredient Specification (2024)

Out of Specification for active ingredient

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Class II

Moderate

FDAApr 17, 2024Nationwide• ARG Laboratories, Inc.

Pain Wizard (ARG Laboratories) – Active Ingredient Violation (2024)

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Class IIModerate

FDAApr 17, 2024Nationwide• ARG Laboratories, Inc.

Pain Wizard (ARG Laboratories) – Active Ingredient Violation (2024)

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Class IIModerate

FDAApr 17, 2024Nationwide• ARG Laboratories, Inc.

Stryker Blueprint Software (Tornier) – case planning bug (2024)

The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant configurations that are incompatible and do not have regulatory approval.

FDAApr 16, 2024Nationwide• Tornier S.A.S. 161 Rue Lavoisier Montbonnot St Martin France

Gordofilm Wart Remover (Gordon Laboratories) – Manufacturing Deviation (2024)

cGMP Deviations

Class IIModerate

FDAApr 12, 2024Nationwide• Dercher Enterprises, Inc., DBA Gordon Laboratories

Island Marinade BBQ Sauce (Detty Family) – Unapproved Process (2024)

No approved scheduled process

Class IIModerate

FDAApr 12, 2024KY, OH• Detty Family Barbeque LTD

Sweet & Smokey BBQ Sauce (Detty Family) – Unapproved Process (2024)

No approved scheduled process

Class IIModerate

FDAApr 12, 2024KY, OH• Detty Family Barbeque LTD

Mildly Spicy BBQ Sauce (Detty Family) – Unapproved Process (2024)

No approved scheduled process

Class IIModerate

FDAApr 12, 2024KY, OH• Detty Family Barbeque LTD

Utility Vehicles (Intimidator) – Crash Hazard (2024)

This recall involves Intimidator and Mahindra branded models 750, 800, 1000, TGB, GC1K and electric utility vehicles (UTVs). The recalled UTVs were sold in a variety of colors. "Intimidator" or "Mahindra" is displayed on the front grill and the model series is printed on the rear-side panels. The serial number can be found on a label inside the glove box, inside the hood compartment and below the driver's seat. The serial range of the recalled Intimidator UTVs is 000000 to 014034. The serial range of the recalled Mahindra UTVs is 000000 to 010545. The following UTVs are included in this recall: Make & Model Model Years: Intimidator GC1K Classic 2018-2023 Intimidator GC1K Crew 2019-2023 Intimidator GC1K Truck 2019-2023 Intimidator 750 Classic 2013-2023 Intimidator 750 Crew 2014-2022 Intimidator 750 Truck 2013-2022 Intimidator 800 Classic 2015-2018 Intimidator 800 Crew Intimidator 800 Enforcer 2016-2018 Intimidator 1000 Diesel Classic 2013-2023 Intimidator 1000 Diesel Crew 2013-2022 Intimidator 1000 Diesel Truck 2013-2023 Intimidator Electric Classic 2013-2023 Mahindra Retriever 750 Classic 2015-2020 Mahindra Retriever 750 Crew 2015-2020 Mahindra Retriever 750 Truck 2015-2020 Mahindra TGB Classic 2015-2020 Mahindra TGB Crew 2015-2020 Mahindra Retriever 1000 Diesel Classic 2015-2020 Mahindra Retriever 1000 Diesel Crew 2015-2020 Mahindra Retriever 1000 Diesel Truck 2015-2020

CPSCApr 11, 2024Nationwide• Intimidator, of Batesville, Ark.

Spectrum IQ Infusion Pump (Baxter) – front panel crack (2024)

There is a potential for cracks on the mount of the front panel of the device.

FDAApr 9, 2024Nationwide• Baxter Healthcare Corporation

Samaritan PAD Defibrillator (HeartSine) – Voice Prompt Malfunction (2024)

Automated external defibrillators have a manufacturing issue that could prevent the device from delivering instructional voice prompts to the user during use of the device. Visual instructional icons will still be present, but this issue could potentially lead to no therapy or a delay in therapy.

FDAApr 8, 2024Nationwide• HeartSine Technologies Ltd 207 Airport Road West Belfast United Kingdom

Sapropterin Dihydrochloride Powder (Dr. Reddy's) – Sub-potent Drug (2024)

Sub-potent Drug; powder discoloration associated with decreased potency

Class IHigh

FDAApr 8, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

Javygtor Oral Powder (Dr. Reddy's) – Sub-potent Drug (2024)

Sub-potent Drug; powder discoloration associated with decreased potency

Class IHigh

FDAApr 8, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

ZirCAD Ceramic Block (Ivoclar) – Sintering Crack Risk (2024)

Defective blocks may show cracks after sintering If cracks are unnoticed, restorations may fracture in the patient's mouth and require restoration

FDAApr 5, 2024Nationwide• IVOCLAR VIVADENT AG BEDERSRASSE LIECHTSTEIN Germany

Evidence MultiSTAT Analyzer (Randox) – Foam Gasket Malfunction (2024)

Foam gasket on the Evidence MultiSTAT chip heater assembly may not perform as expected. Foam that is not functioning as expected may cause light to leak into the Charged Coupled Device (CCD) Camera during imaging. This will affect the testing and may delay in reporting results.

FDAApr 5, 2024Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Tide Pods (Procter & Gamble) – Defective Packaging (2024)

This recall involves certain lot codes of Tide Pods, Gain Flings, Ace Pods, and Ariel Pods liquid laundry detergent packets packaged in flexible film bags that were manufactured between September 2023 and February 2024. Recalled products range from bags with 12 to 39 laundry detergent packets and include the following: Gain Flings Original Tide Simply Pods Plus Oxi Boost Gain Flings Moonlight Breeze Scent Tide Pods Clean Breeze Scent Gain Flings Blissful Breeze Scent Tide Pods Free & Gentle Gain Flings Spring Daydream Scent Tide Pods Oxi Gain Flings Plus Ultra Oxi Tide Pods Ultra Oxi Gain Flings Plus Odor Defense Ace Pods Clean Breeze Tide Pods Original Ace Pods Spring Meadow Tide Pods Spring Meadow Scent Ariel Pods Alpine Breeze Tide Pods Light

CPSCApr 5, 2024Nationwide• The Procter & Gamble Company, of Cincinnati, Ohio

IntelliSpace Cardiovascular Software (Philips) – Data Export Issue (2024)

Study data is not able to be archived, copied, or exported with the cardiovascular software version.

FDAApr 4, 2024Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Urinalysis Test Strips (Macherey Nagel) – Missing Test Pad (2024)

The reason for the recall is one of the test pads, for the parameter leukocytes, was missing on some of the test strips. The issue was identified by a consumer by way of a Henry Schein Inc. (HSI) customer complaint. This problem can potentially result in the possibility that the parameter leucocytes (a non-specific marker for urinary track infections and an indicator for inflammatory renal processes) is interpreted instrumentally as a false negative. The following HSI item number and lot number were affected: Urispec 11-Way, #102-2285, LOT 65402.

FDAApr 4, 2024Nationwide• Macherey Nagel Gmbh & Co. Kg Valencienner Str. 11 Duren Germany