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Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods

Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods Recalls

All product recalls associated with Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods.

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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 301–320 of 7756 recalls

Sukhi's Tikka Masala Curry Paste – Metal Contamination (2025)

Potential contamination with foreign objects (metal pieces).

Class IIModerate

FDAJul 23, 2025AZ, AR, CA +30 more• Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods

Sukhi's Classic Curry Sauce – Metal Contamination (2025)

Potential contamination with foreign objects (metal pieces).

Class IIModerate

FDAJul 23, 2025AZ, AR, CA +30 more• Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods

Relaxation Tea (Herbalife) – Ingredient Error (2025)

Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.

Class II

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Moderate

FDAJul 21, 2025Nationwide• Herbalife International of America

Amlodipine Olmesartan Tablets (Ascend) – Dissolution Failure (2025)

Failed Dissolution Specifications: low dissolution results

Class IIModerate

FDAJul 21, 2025Nationwide• Ascend Laboratories, LLC

Celsite BabyPort Set (B.Braun) – Minor Injury Potential (2025)

The potential for minor injury such as damage to the vessel and/or tearing of the vessel wall.

FDAJul 21, 2025Nationwide• B.Braun Medical S.A.S. Celsa Lg Medical 30 avenue des Temps Modernes; Cs 10031 Chasseneuil du Poitou CEDEX France

TOPS Inserter (Premia Spine) – Missing Pin Risk (2025)

Potential for missing pins at tip of inserter.

FDAJul 16, 2025Nationwide• PREMIA SPINE LTD Giborey Israel 7 Ramat Poleg Netanya Israel

Duloxetine Capsules (Breckenridge Pharmaceutical) – Impurity Concern (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety assessment limit

Class IIModerate

FDAJul 15, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

Corin Operating Tables (Maquet) – Device Interference Risk (2025)

Under certain conditions, such as the simultaneous use of the operating table with other medical devices, including high-frequency (HF) surgical equipment, interference may occur that could prevent the device from performing as intended. If the issue occurs, the operating table is unresponsive to command from both the universal remote control and override panel.

FDAJul 14, 2025Nationwide• MAQUET GMBH Kehler Str. 31 Rastatt Germany

3mensio Workstation (PIE Medical) – Measurement Error (2025)

When fenestrated analysis with clock measurements is started in diagnostic bioimaging software (intended to measure/visualize cardiovascular structures) and the 12h position of a single clock is changed, other clock measurements are not updated relative to the new 12h position which may cause stent graft fenestrations at incorrect position, which may lead to blood flow disruption and tissue damage

FDAJul 14, 2025Nationwide• PIE Medical Imaging B.V. Demertdwarsstraat 8A01 Maastricht Netherlands

Spectrum IQ Infusion Pump (Baxter) – Grease Breakdown (2025)

Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down quickly. The breakdown of the grease will lead to the device having insufficient or ineffective grease applied to the cam, which could lead to premature wear of the mechanism assembly, resulting in excessive therapy.

FDAJul 14, 2025AZ, FL• Baxter Healthcare Corporation

Baxter Novum IQ Pump (Baxter) – Infusion Transition Risk (2025)

Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large volume pump (LVP) due to the potential for underinfusion when transitioning from a flow rate to a higher flow rate that is more than double. (e.g., rate change or bolus). The level of underinfusion is variable based on the current infusion rate, the duration the pump has been running at this flow rate, and the magnitude of the rate change. The longer the duration the pump has been running at the current infusion rate and the larger the magnitude of the rate change, the larger the underinfusion that would be experienced. Additionally, Baxter has identified an increase in customer reports of over and underinfusion potentially due to set misloading. Failure to properly load the tubing into the pump channel may result in the pump infusing at a rate higher or lower than programmed. Consistent with the instructions for use, customers should ensure that: 1) The door is fully open before loading the set. 2) The tubing is taut and loaded without slack in the pumping channel.

FDAJul 14, 2025Nationwide• Baxter Healthcare Corporation

Malibu Boat Trailer (Malibu Boats) – Brake Line Fracture (2025)

Malibu Boats, LLC (Malibu Boats) is recalling certain 2021-2026 Triple Axle Boat Trailers. The brake line may fracture at the connection point to the caliper, causing a loss of brake function.

NHTSAJul 11, 2025Nationwide• MALIBU BOATS

Sucralfate Tablets (Nostrum Laboratories) – Quality Program Disruption (2025)

CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.

Class IIModerate

FDAJul 11, 2025Nationwide• Nostrum Laboratories, Inc.

Micro Joystick R-net (mo-Vis) – Software Timing Error (2025)

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

FDAJul 10, 2025Nationwide• mo-Vis BVBA Biebuyckstraat 15D Nevele Belgium

Access Thyroglobulin Assay (Beckman Coulter) – Result Inaccuracy (2025)

Access Thyroglobulin reagent lot 439163 may generate erroneously high patient results. Falsely increased Access Thyroglobulin results may lead a physician to pursue unnecessary diagnostic imaging studies and/or inappropriate therapy adjustments in patients being monitored for residual or recurrent thyroid cancer.

FDAJul 10, 2025Nationwide• Beckman Coulter, Inc.

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Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods Recalls

Recall Summary

Sukhi's Tikka Masala Curry Paste – Metal Contamination (2025)

Sukhi's Classic Curry Sauce – Metal Contamination (2025)

Relaxation Tea (Herbalife) – Ingredient Error (2025)

Amlodipine Olmesartan Tablets (Ascend) – Dissolution Failure (2025)

Celsite BabyPort Set (B.Braun) – Minor Injury Potential (2025)

TOPS Inserter (Premia Spine) – Missing Pin Risk (2025)

Duloxetine Capsules (Breckenridge Pharmaceutical) – Impurity Concern (2025)

Corin Operating Tables (Maquet) – Device Interference Risk (2025)

3mensio Workstation (PIE Medical) – Measurement Error (2025)

Spectrum IQ Infusion Pump (Baxter) – Grease Breakdown (2025)

Baxter Novum IQ Pump (Baxter) – Infusion Transition Risk (2025)

Malibu Boat Trailer (Malibu Boats) – Brake Line Fracture (2025)

Sucralfate Tablets (Nostrum Laboratories) – Quality Program Disruption (2025)

Micro Joystick R-net (mo-Vis) – Software Timing Error (2025)

R-net Light Joystick (mo-Vis) – Software Timing Error (2025)

IDM-ARLITE-R (mo-Vis) – Software Timing Error (2025)

Multi Joystick R-net (mo-Vis) – Software Timing Error (2025)

IDM-MULTI-R (mo-Vis) – Software Timing Error (2025)

IDM-MICRO-R (mo-Vis) – Software Timing Error (2025)

Access Thyroglobulin Assay (Beckman Coulter) – Result Inaccuracy (2025)