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. 2,915 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,915 in last 12 months

Showing 89018920 of 55,304 recalls

DrugAugust 2, 2023· Parker Laboratories, Inc.

Recalled Item: Helix CBD Therapy Cream (Menthol 7.4%) Recalled by Parker Laboratories, Inc....

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2023· Parker Laboratories, Inc.

Recalled Item: Helix CBD Clinical Cream (Menthol 7.4%) Recalled by Parker Laboratories,...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2023· Parker Laboratories, Inc.

Recalled Item: Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%) Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2023· Pearson Foods Corporation

Recalled Item: Pearson Foods Lettuce Romaine. 1 Recalled by Pearson Foods Corporation Due...

The Issue: Potentially contaminated with deer feces

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2023· RMJV, LP dba Fresh Creative Foods

Recalled Item: Fresh Creative Foods Caesar Salad Kit Recalled by RMJV, LP dba Fresh...

The Issue: Product potentially contaminated with deer feces

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 2, 2023· Philips Healthcare

Recalled Item: Incisive CT Recalled by Philips Healthcare Due to Philips has identified...

The Issue: Philips has identified three software issues with compliance concerns to...

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

Class II — Potential Health HazardOngoing
FoodAugust 1, 2023· Lipari Foods Operating Company, LLC.

Recalled Item: IO Inspired Organics brand Organic Raw Walnut Halves & Pieces Recalled by...

The Issue: undeclared walnuts in ingredient and contains statement

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

Class III — Low RiskOngoing
Refund
FoodAugust 1, 2023· C&E Farms, Inc.

Recalled Item: Romaine lettuce packed in bulk 45-lb mini-bins Recalled by C&E Farms, Inc....

The Issue: Product potentially contaminated with deer feces

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2023· SynCardia Systems LLC

Recalled Item: SynCardia 50cc TAH-t Recalled by SynCardia Systems LLC Due to Artificial...

The Issue: Artificial hearts contain a epoxy resin that has not been reviewed by the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2023· Skytron, LLC

Recalled Item: GS70H Salus Surgical Table Recalled by Skytron, LLC Due to When the control...

The Issue: When the control of the operating table was used in Bluetooth mode, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2023· Skytron, LLC

Recalled Item: GS70 Salus Surgical Table Recalled by Skytron, LLC Due to When the control...

The Issue: When the control of the operating table was used in Bluetooth mode, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2023· B. Braun Medical, Inc.

Recalled Item: Perifix¿ / Epidural anesthesia set Recalled by B. Braun Medical, Inc. Due to...

The Issue: Product may be mislabeled with an incorrect lid stock label.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The...

The Issue: The incorrect product labeling was applied to the product indicating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were reporting that the device was not charging as expected. It was...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users reported "System Over Temperature" alarms associated with a loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were reporting that the device was not charging as expected. It was...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were identifying autofill failure conditions on the devices causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users reported "System Over Temperature" alarms associated with a loss of...

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

Class I — Serious Health HazardOngoing