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JABSONS FOODS PRIVATE LIMITED (Formerly Known as Jabsons Cottonseed Ind.Pvt.Ltd.)

JABSONS FOODS PRIVATE LIMITED (Formerly Known as Jabsons Cottonseed Ind.Pvt.Ltd.) Recalls

All product recalls associated with JABSONS FOODS PRIVATE LIMITED (Formerly Known as Jabsons Cottonseed Ind.Pvt.Ltd.).

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Recall Summary

Total Recalls

1000

Past Year

566

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 1321–1340 of 7756 recalls

Page 67 of 388Next

Device suddenly and forcefully disassembled after cryotherapy, potential for long-term or permanent impairment of a patient or user if a CryoTreq device suddenly or forcefully disassembles during a cryosurgery procedure.

FDAMar 17, 2023Nationwide• Beaver Visitec International, Inc.

Aripiprazole Tablets (Ascend Laboratories) – Spectroscopic Test Failure (2023)

Out of specification (OOS) for Spectroscopic Identification test by IR.

Class IIModerate

FDAMar 17, 2023Nationwide• Ascend Laboratories, LLC

Nurtec ODT (Pfizer) – Packaging Safety Issue (2023)

This recall involves prescription drugs Nurtec ODT 75 mg orally disintegrating tablets sold in cartons containing one blister card of 8 tablets. The tablets are in a non-child resistant blister card packaged in a carton that includes the name of the product, dosage strength, expiration date. The dosage strength and expiration date are printed or stamped on the blister card. The recall includes the following: Product Description NDC Number Expiration Date Nurtec® ODT (rimegepant) 75mg 8-Unit Dose blister pack 72618-3000-2 All dates through 6/2026

CPSCMar 16, 2023Nationwide• Biohaven Pharmaceuticals Inc., of New Haven, Conn.

Fredericksburg Candles – Laceration Risk (2023)

Laceration Risk

This recall involves 10-ounce Scented Candles in a square glass jar with a glass lid. The model number and UPC code are printed on the label on the bottom of the jar. Fredericksburg Farms is printed on the front of the jar The following 15 scents of candles are included in the recall: The bag containing potassium hydroxide has a blue label with "POTASSIUM HYDROXIDE FLAKES." Model # Scent UPC Code D2001A West Texas Saddle Leather, 10 oz. 8 00565 80822 2 D2009A Buttery Vanilla, 10 oz. 8 00565 80826 0 D2011A Creme Brulee, 10 oz. (Small) 8 00565 80828 4 D2012A Spiced Orange, 10 oz. (Small) 8 00565 80830 7 D2013A Hill Country Christmas, 10 oz. (Small) 8 00565 80832 1 D2017A Bird of Paradise, 10 oz. (Small) 8 00565 80834 5 D2025A Hill Country Lavender, 10 oz. (Small) 8 00565 80840 6 D2042A Sandalwood Currant, 10 oz. (Small) 8 00565 80854 3 D3100A Texas Ruby Red Grapefruit, 10 oz. (Small) 8 00565 80856 7 D3101A Autumn Harvest, 10 o. 8 00565 80858 1 D3111A Spiced Chestnut, 10 oz. (Small) 8 00565 80876 5 D3112A Snowy Mountain Lodge, 10 oz. (Small) 8 00565 80877 2 D3113A Peppercorn & Ginger, 10 oz. (Small) 8 00565 80878 9 D3115A Teakwood & Mahogany, 10 oz. (Small) 8 00565 80880 2 D3116A Vanilla Birch, 10 oz. (Small) 8 00565 80881 9

CPSCMar 16, 2023Nationwide• Fredericksburg Distribution, dba Fredericksburg Farms, of Fredericksburg, Texas

STIHL iMOW Docking Stations – Fire Hazard (2023)

Fire/Burn Risk

This recall involves the docking station supplied with the STIHL iMOW, an autonomous battery-powered lawn mower. The docking stations are gray and orange. "iMOW" is displayed on the top of the mower and "STIHL" is displayed on the top of the mower and the top of the docking station. The recalled docking station's serial number is located on a label at the base of the docking station. The following models and serial numbers are included in this recall. Name Model Numbers iMow Serial Numbers Range Docking Station Serial Numbers Range STIHL iMOW RMI 422 RMI 522 RMI 632 437478902 to 443268968 437475057 to 443268971

CPSCMar 16, 2023Nationwide• STIHL Tirol GmbH, of Austria

Beckman Coulter Access Free T3 (Beckman Coulter) – test result issue (2023)

The reagent lot produces elevated results (approximately >30%) in some (15-20%)patient samples that do not correlate with the results of other thyroid markers nor Free T3 results generated on other platforms. This introduces a risk of the positive bias not being detected by QC with the potential that clinical correlation with other thyroid function tests will be inconsistent requiring additional testing; however the clinical assessment and treatment decisions are not made in isolation on a single test result especially, in the setting of thyroid function testing. False positive test results could lead to a euthyroid patient being interpreted clinically as having elevated thyroid function (hyperthyroid) or a hypothyroid patient being within the normal range. Such misdiagnoses may lead to inappropriate treatment of a euthyroid patient with anti-thyroid medications or hypothyroid patient not getting sufficient treatment since their free T3 test result demonstrates them to be in the euthyroid range.

FDAMar 15, 2023Nationwide• Beckman Coulter, Inc.

Dianeal Low Calcium Dialysis Solution (Baxter Healthcare) – Sterility Concern (2023)

Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Class IIModerate

FDAMar 15, 2023Nationwide• Baxter Healthcare Corporation

Dianeal PD-2 Dialysis Solution (Baxter Healthcare) – Sterility Concern (2023)

Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Class IIModerate

FDAMar 15, 2023Nationwide• Baxter Healthcare Corporation

Hamilton-C6 Ventilator (Hamilton Medical) – safety ventilation error (2023)

Software error causes, safety ventilation, in which ventilation continues in the "safety ventilation" mode with audible/visible alarm - patient inputs are not monitored, if the following coincide 1) A mode change to an adaptive mode (ASV, APVcmv, APVsimv, INTELLiVENT-ASV, (S)CMV+, SIMV+), and 2) The controller and/or humidifier is connected to the ventilator and is operational.

FDAMar 14, 2023Nationwide• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Dabigatran Etexilate Capsules (Ascend Laboratories) – Impurity Levels (2023)

CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.

Class IIModerate

FDAMar 14, 2023Nationwide• Ascend Laboratories, LLC

Dabigatran Etexilate Capsules (Ascend Laboratories) – Impurity Levels (2023)

CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.

Class IIModerate

FDAMar 14, 2023Nationwide• Ascend Laboratories, LLC

Atovaquone Oral Suspension 750mg (Camber) – Microbial Contamination (2023)

Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.

Class IHigh

FDAMar 13, 2023Nationwide• Camber Pharmaceuticals Inc.

Matiz Piparra Peppers (Culinary Collective) - Glass Shard (2023)

A shard of glass being found in one of the jars.

Class IIModerate

FDAMar 13, 2023IL, IN, IA +4 more• Power Selles Imports dba Culinary Collective

Quantum Perfusion Systems (Spectrum Medical) – bobbin lock fault (2023)

The ratchet and pawl had an out of tolerance geometry which exhibited as the left bobbin would not lock.

FDAMar 13, 2023Nationwide• Spectrum Medical Ltd. Harrier 4, Meteor Business Park Cheltenham Road East Gloucester United Kingdom

DeVilbiss Healthcare Oxygen Concentrator (DeVilbiss) – Manual Update (2023)

The instruction manual is being replaced with an updated version that is in alignment with labeling requirements specified in the IEC-60101-1 standard.

FDAMar 9, 2023Nationwide• DeVilbiss Healthcare LLC

Jardiance 25mg Tablets (Boehringer) – Label Mix-up (2023)

Labeling: Label Mix-up

Class IIModerate

FDAMar 9, 2023Nationwide• Boehringer Ingelheim Pharmaceuticals, Inc.

FilmArray GI Panel (BioFire) – False Negative Results (2023)

Due to manufacturing issue, Gastrointestinal (GI) Panel may result in false negative results.

FDAMar 8, 2023Nationwide• BioFire Diagnostics, LLC

REX Pressure Therapy System (Compass Health) – User Manual Error (2023)

Error in the Introduction section of the user manual that indicates the device may be used for the prevention of deep vein thrombosis (DVT). Marketed without a 510k for this indication

FDAMar 7, 2023Nationwide• Compass Health Brands (Corporate Office)

Stay Informed

JABSONS FOODS PRIVATE LIMITED (Formerly Known as Jabsons Cottonseed Ind.Pvt.Ltd.) Recalls

Recall Summary

Tandoori Roasted Peanut (Jabsons) – Undeclared Milk (2023)

Tandoori Cashew Nuts (Jabsons) – Undeclared Milk (2023)

CryoTreQ Surgical Device (Beaver Visitec) – disassembly risk (2023)

Aripiprazole Tablets (Ascend Laboratories) – Spectroscopic Test Failure (2023)

Nurtec ODT (Pfizer) – Packaging Safety Issue (2023)

Fredericksburg Candles – Laceration Risk (2023)

STIHL iMOW Docking Stations – Fire Hazard (2023)

Beckman Coulter Access Free T3 (Beckman Coulter) – test result issue (2023)

Dianeal Low Calcium Dialysis Solution (Baxter Healthcare) – Sterility Concern (2023)

Dianeal PD-2 Dialysis Solution (Baxter Healthcare) – Sterility Concern (2023)

Hamilton-C6 Ventilator (Hamilton Medical) – safety ventilation error (2023)

Dabigatran Etexilate Capsules (Ascend Laboratories) – Impurity Levels (2023)

Dabigatran Etexilate Capsules (Ascend Laboratories) – Impurity Levels (2023)

Atovaquone Oral Suspension 750mg (Camber) – Microbial Contamination (2023)

Matiz Piparra Peppers (Culinary Collective) - Glass Shard (2023)

Quantum Perfusion Systems (Spectrum Medical) – bobbin lock fault (2023)

DeVilbiss Healthcare Oxygen Concentrator (DeVilbiss) – Manual Update (2023)

Jardiance 25mg Tablets (Boehringer) – Label Mix-up (2023)

FilmArray GI Panel (BioFire) – False Negative Results (2023)

REX Pressure Therapy System (Compass Health) – User Manual Error (2023)