Product Recalls in Illinois

Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,733 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,733 in last 12 months

Showing 2646126480 of 55,304 recalls

Medical DeviceAugust 31, 2018· Accuray Incorporated

Recalled Item: Ashland(TM) Box Film Ball Cube II EBT3 Recalled by Accuray Incorporated Due...

The Issue: the Ball Cube II phantom calibration film was not manufactured within...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Arrow International Inc

Recalled Item: Arrow AGB + Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...

The Issue: The product was shipped after its expiry date due to a system error. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Mitek Screw and Washer Depth Gauge Recalled by DePuy Mitek, Inc., a Johnson...

The Issue: The device has an offset in the design that results in a reading...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodAugust 29, 2018· Cedarlane Natural Foods Inc/Frankly Fresh Foods Inc.

Recalled Item: CedarLane Organic Salads Recalled by Cedarlane Natural Foods Inc/Frankly...

The Issue: Discovery that the product is labeled as gluten free but contains wheat...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2018· Humco Holding Group, Inc

Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...

The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2018· Humco Holding Group, Inc

Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...

The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2018· Humco Holding Group, Inc

Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...

The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2018· Pfizer Inc.

Recalled Item: Argatroban Injection Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification stability...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 28, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...

The Issue: There is a potential to generate falsely elevated serum or plasma chloride...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...

The Issue: The reagent pack exhibits the potential for an increased frequency of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing