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 89218940 of 55,304 recalls

Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Rescue 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 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 Hybrid 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
FoodJuly 28, 2023· California Ranch Food Company, Inc.

Recalled Item: Trader Joe's Fully Cooked Falafel Heat & Eat NET WT. Recalled by California...

The Issue: Foreign object; rocks.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2023· ALEMBIC PHARMACEUTICALS, INC.

Recalled Item: Tobramycin Opthalmic Solution USP Recalled by ALEMBIC PHARMACEUTICALS, INC....

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing