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. 1,044 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,044 in last 12 months

Showing 37761–37780 of 55,304 recalls

Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Centimeter Sizing Catheter Beacon Tip White Vessel Sizing...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: White Lumax Guiding Coaxial Catheter Catheter Recalled by Cook Inc. Due to...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Haskal Transjugular Intrahepatic Portal Access Set Introducer Recalled by...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Ziehm Imaging Inc

Recalled Item: Ziehm Vision RFD Mot Recalled by Ziehm Imaging Inc Due to Malfunction of the...

The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Ziehm Imaging Inc

Recalled Item: Ziehm Vision R Recalled by Ziehm Imaging Inc Due to Malfunction of the...

The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Torcon NB Advantage Catheter Catheter Recalled by Cook Inc. Due...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: FluoroSet Radiographic Tubal Assessment Set Cannula Recalled by Cook Inc....

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Ziehm Imaging Inc

Recalled Item: Ziehm Solo Recalled by Ziehm Imaging Inc Due to Malfunction of the...

The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IG1 Recalled by Siemens Healthcare Diagnostics, Inc. Due to 24 minutes of...

The Issue: 24 minutes of incubation is required prior to processing patient samples and...

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

Class II — Potential Health HazardOngoing
FoodApril 15, 2016· FoodState, Inc

Recalled Item: MegaFood Multi for Women 40+ Recalled by FoodState, Inc Due to Multi Vitamin...

The Issue: Multi Vitamin label fails to have required warning statement for iron and...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2016· Health 4 Life, LLC

Recalled Item: Passion 4 Life 30 FL oz. Bottle Recalled by Health 4 Life, LLC Due to...

The Issue: Undeclared whey protein containing the allergens of milk and soy lecithin.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V4 Recalled by Carestream Health Inc Due to...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Covidien LLC

Recalled Item: Given Imaging Bravo¿ pH capsule delivery device Recalled by Covidien LLC Due...

The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...

The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...

The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Covidien LLC

Recalled Item: Given Imaging Bravo¿¿ pH capsule delivery device Recalled by Covidien LLC...

The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Biosense Webster, Inc.

Recalled Item: Pentaray NAV High-Density Mapping ECO Catheter Recalled by Biosense Webster,...

The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Dynamics Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens has identified changes in default carry forward workflow using...

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

Class II — Potential Health HazardOngoing