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The Candy Basket Inc

The Candy Basket Inc Recalls

All product recalls associated with The Candy Basket 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 561–580 of 7756 recalls

Lemon Jelly Sticks WHITE (The Candy Basket) – Undeclared Additives (2025)

Undeclared Allergen

Undeclared Yellow #5 and Potassium Sorbate.

Class IIModerate

FDAJan 15, 2025CA, IN, OR +1 more• The Candy Basket Inc

Lemon Jelly Sticks DARK (The Candy Basket) – Undeclared Additives (2025)

Undeclared Allergen

Undeclared Yellow #5 and Potassium Sorbate.

Class IIModerate

FDAJan 15, 2025CA, IN, OR +1 more• The Candy Basket Inc

Raspberry Jelly Sticks MILK (The Candy Basket) – Undeclared Additives (2025)

Undeclared Allergen

Undeclared Red #40 and Potassium Sorbate.

1...27 282930 31...388

Page 29 of 388Next

Class IIILow

FDAJan 15, 2025CA, IN, OR +1 more• The Candy Basket Inc

Orange Jelly Sticks (Candy Basket) – Undeclared Additives (2025)

Undeclared Allergen

Undeclared Yellow #6, and Sodium Benzoate.

Class IIModerate

FDAJan 15, 2025CA, IN, OR +1 more• The Candy Basket Inc

Orange Jelly Sticks DARK (The Candy Basket) – Undeclared Additives (2025)

Undeclared Allergen

Undeclared Yellow #6, and Sodium Benzoate.

Class IIModerate

FDAJan 15, 2025CA, IN, OR +1 more• The Candy Basket Inc

Raspberry Jelly Sticks DARK (The Candy Basket) – Undeclared Additives (2025)

Undeclared Allergen

Undeclared Red #40 and Potassium Sorbate

Class IIILow

FDAJan 15, 2025CA, IN, OR +1 more• The Candy Basket Inc

Duloxetine Capsules (Harvard Drug Group) – Nitrosamine Impurity (2025)

CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity (NDSRI), N-Nitroso-Duloxetine above the FDA recommended acceptable intake limit

Class IIModerate

FDAJan 13, 2025Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Nobel Biocare N1 TiUltra (Nobel) – Packaging Defect (2025)

Due to manufacturing issue (unintended by-product of the injection molding process) a sharp pin that may puncture the blister packaging and breaching the sterile barrier of the finished product.

FDAJan 10, 2025Nationwide• Nobel Biocare Vastra Hamngatan 1 Goteborg Sweden

DxC 500 AU Analyzer (Beckman) – Stability Date Issue (2025)

Beckman Coulter has identified an issue which prevents the DxC 500 AU instrument from providing the correct onboard stability (Open Expiration) dates for assays that were loaded prior to a software upgrade (e.g. 1.3 to 1.4, 1.4 to 1.4.1, etc.). As a result, assays that have expired may still be used for sample processing, leading to inaccurate or erroneous patient test results. The issue only happens on assays loaded before instruments doing upgrades and does not impact new installation. It does not impact the assays loaded after upgrade.

FDAJan 10, 2025AL, CA, CO +16 more• BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD. No.

Soft Plum (AAHU BARAH) – Undeclared Sulfites (2025)

Undeclared Allergen

Product contains undeclared sulfites (4.66 mg/serving).

Class IIModerate

FDAJan 9, 2025CO, FL, GA +10 more• Global Commodities Inc

MSOT Acuity Echo (Ithera) – Safety Instruction (2025)

The MSOT Acuity Echo does not include an adequate instruction for safe operation of the device. The previous version of the user manuals contained a wrong value for the Nominal Ocular Hazard Distance (NOHD).

FDAJan 8, 2025Nationwide• Ithera Medical Gmbh Zielstattstr. 13 Munich Germany

Guaifenesin Codeine Solution (PAI Holdings) – Superpotent Preservative (2025)

Superpotent; sodium benzoate preservative

Class IIILow

FDAJan 7, 2025OH• PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Organic Almonds (Woodstock) – Mislabeled Product (2025)

Product mislabeled. The back label states Organic Cashews. The front product label states Wegmans Organic unsalted dry roasted almonds. The front label is correct label for this product.

Class IIModerate

FDAJan 6, 2025NY, PA, VA• United Natural Trading Inc. dba Woodstock Farms

Dierbergs Kitchen Mac & Cheese (Dierbergs Markets) – Mislabeled Allergens (2025)

Undeclared Allergen

Undeclared allergens (wheat) on label, incorrect label was placed on product

Class IIModerate

FDAJan 3, 2025IL, IN, MO• Dierbergs Markets, Inc.

Cairo Bakery Pita Pocket Bread (Middle East Baking Co.) – Undeclared Milk (2025)

Undeclared Milk

Undeclared milk

Class IHigh

FDAJan 3, 2025CA• Middle East/ Soli's Baking Company, Inc. dba Middle East Baking Co.

Access PCT Reagent Pack (Beckman) – Calibration Failure (2025)

Identified reagent lots are experiencing a high rate of calibration failures with failure code of "Max Iterate" on Access 2 and UniCel Dxl Immunoassay Systems. Reporting of results may be delayed due to the time required to achieve a passing calibration curve.

FDAJan 2, 2025Nationwide• Beckman Coulter Inc.

Lev5 Susceptibility Discs (Oxoid) – Mislabeling Risk (2024)

Mislabeling; Levofloxacin Antimicrobial susceptibility disc packaging may contain Norfloxacin Antimicrobial Susceptibility discs.

FDADec 23, 2024CA, FL, MA +4 more• Oxoid Limited Wade Road Basingstoke United Kingdom

Ultra Repair Cream (First Aid Beauty) – distribution error (2024)

CGMP Deviations; product intended for quarantine was inadvertently distributed

Class IIModerate

FDADec 23, 2024Nationwide• First Aid Beauty Ltd

Life 2000 Ventilation System (Baxter) – Battery Charger Alarm (2024)

There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.

FDADec 20, 2024Nationwide• Baxter Healthcare Corporation

Life2000 Ventilation System (Baxter) – Battery Charger Alarm (2024)

There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.

FDADec 20, 2024Nationwide• Baxter Healthcare Corporation