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Windy Hill Chocolate LLC

Windy Hill Chocolate LLC Recalls

All product recalls associated with Windy Hill Chocolate LLC.

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Recall Summary

Total Recalls

1000

Past Year

593

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 1781–1800 of 10391 recalls

Peanut Butter Praline (Windy Hill Chocolate) – Allergen Risks (2023)

Undeclared Allergen

Undeclared Allergens: Soy, Milk and Tree Nuts

Class IIModerate

FDAMar 22, 2023Nationwide• Windy Hill Chocolate LLC

Philips Azurion System (Philips) – X-ray functionality loss (2023)

Potential Loss of X-ray-When the full disk capacity is reached, X-Ray functionality will cease to be available there will be a sudden interruption of the procedure

FDAMar 21, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

ExactaMed Oral Dispenser (Baxter) – particulate matter risk (2023)

ExataMed 20 mL oral dispenser component of the Clear Pharmacy Pack may have particulate matter.

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FDAMar 20, 2023Nationwide• Baxter Healthcare Corporation

Philips Incisive CT System (Philips) – foot switch entrapment (2023)

Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and injury

FDAMar 20, 2023Nationwide• Philips North America

Spectral CT 7500 System (Philips) – foot switch entrapment (2023)

Laceration Risk

Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operators foot. If foot or leg entrapment occurs while pressing Unload Pedal, the risk to operators may include: pain, muscle or ligament sprain, abrasion, laceration, contusion, fracture, loss of function, and joint dislocation.

FDAMar 17, 2023Nationwide• Philips North America Llc

Glimepiride 4mg Tablets (Amerisource) – Manufacturing Deviation (2023)

CGMP Deviations: recalling drug products following an FDA inspection.

Class IIModerate

FDAMar 17, 2023Nationwide• Amerisource Health Services LLC

Glimepiride Tablets (Amerisource Health Services) – Manufacturing Deviation (2023)

CGMP Deviations: recalling drug products following an FDA inspection.

Class IIModerate

FDAMar 17, 2023Nationwide• Amerisource Health Services LLC

Glimepiride Tablets (Amerisource Health Services) – Manufacturing Deviation (2023)

CGMP Deviations: recalling drug products following an FDA inspection.

Class IIModerate

FDAMar 17, 2023Nationwide• Amerisource Health Services LLC

Atellica IM Cortisol Test (Siemens) – urine sample bias (2023)

There is a negative bias with urine patient samples and urine cortisol Quality Control (QC) results intermittently out of range low.

FDAMar 16, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

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.

ADVIA Centaur Cortisol Test (Siemens) – urine sample bias (2023)

There is a negative bias with urine patient samples and urine cortisol Quality Control (QC) results intermittently out of range low.

FDAMar 16, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

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