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CON YEAGER SPICE CO.

CON YEAGER SPICE CO. Recalls

All product recalls associated with CON YEAGER SPICE CO..

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Recall Summary

Total Recalls

1000

Past Year

1000

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 1601–1620 of 21319 recalls

Trail Bologna Processing Kit (Con Yeager) – Undeclared Allergens (2024)

Undeclared Allergen

Undeclared Allergen - Wheat and Soy

Class IHigh

FDAOct 11, 2024IL, KY, MD +7 more• CON YEAGER SPICE CO.

Vue PACS Viewer (Philips) – Calculation Errors (2024)

A software issue affecting Philips Vue PACS may cause incorrect ischemic map and table value calculations when using the export function in the Perfusion Application for a Siemens CT perfusion study, resulting in misdiagnosis due to incorrect ischemic map and table values.

High

FDAOct 10, 2024Nationwide• Philips Medical Systems Technologies Ltd. Matam Building 8/2 Advanced Technology Center Haifa Israel

Boston Scientific POLARx Balloon Catheter (Boston Scientific) – Use Instructions (2024)

Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.

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Moderate

FDAOct 10, 2024Nationwide• Boston Scientific Corporation

BioZorb Marker (Hologic) – Adverse Event Risk (2024)

Firm received reports of adverse events/complications that include serious injuries, such as pain, infection, rash, device migration, device erosion, seroma, and discomfort.

High

FDAOct 10, 2024Nationwide• Hologic, Inc

Boston Scientific POLARx Balloon Catheter (Boston Scientific) – Use Instructions (2024)

Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.

Moderate

FDAOct 10, 2024Nationwide• Boston Scientific Corporation

Boston Scientific SmartFreeze Cryo Console (Boston Scientific) – Use Instructions (2024)

Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.

Moderate

FDAOct 10, 2024Nationwide• Boston Scientific Corporation

BBQ Pulled Chicken Sandwich (Whitsons) – Listeria contamination (2024)

Listeria

Product may be contaminated with Listeria monocytogenes.

Class IIModerate

FDAOct 10, 2024NY• Whitsons Food Service (Bronx), LLC

Duloxetine Capsules (Breckenridge) – Nitrosamine Impurity (2024)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

Class IIModerate

FDAOct 10, 2024Nationwide• Breckenridge Pharmaceutical, Inc

MONOCRYL Suture (ETHICON) – Component Mix-Up Risk (2024)

Due a component mix-up in manufacturing, the affected products may contain incorrect needle type/size and suture length.

Moderate

FDAOct 8, 2024AL, AK, AZ +42 more• ETHICON, INC. Calle Durango 2751 Col. Parque Industrial Americas, Juarez Juarez Mexico

AK Forte Tablets (C & A) – Undeclared Ingredients (2024)

Undeclared Allergen

Marketed without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared diclofenac and acetaminophen.

Class IIModerate

FDAOct 8, 2024Nationwide• C & A Naturistics

Garbin Evo Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

Low

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Trilogy EV300 Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

Low

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Trilogy Evo Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

Low

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Philips Zenition 70 (PHILIPS) – Mains Control Unit Fuse Issue (2024)

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

High

FDAOct 7, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Trilogy Evo Universal Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

Low

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Trilogy Evo O2 Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

Low

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Aeris EVO Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

Low

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

Philips Zenition 50 (PHILIPS) – Mains Control Unit Fuse Issue (2024)

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

High

FDAOct 7, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

LifeVent EVO2 Ventilator (Philips) – Nebulizer Flow Sensor Issue (2024)

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

Low

FDAOct 7, 2024Nationwide• Philips Respironics, Inc.

CardioMEMS HF System (St. Jude Medical) – Cloud Data Migration Error (2024)

As a result of a cloud data migration of Patient and Hospital Electronic Systems (PES and HES) reverted to an outdated configuration causing incorrect/inaccurate pulmonary artery (PA) pressure readings.

High

FDAOct 5, 2024Nationwide• St. Jude Medical