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 3002130040 of 55,304 recalls

Medical DeviceNovember 14, 2017· Carl Zeiss Metrology Inc

Recalled Item: Metrotom 800 (130kV CT scanner) Industrial CT scanner for measuring Recalled...

The Issue: Due to a software error, it was observed that when the user closes the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy Programmer Recalled by Cyberonics, Inc Due to Certain Model 3000...

The Issue: Certain Model 3000 programming events can result in miscalculation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 3500 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
DrugNovember 11, 2017· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Superpotent

The Issue: Superpotent

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

Class III — Low RiskOngoing
Refund
FoodNovember 11, 2017· Bush Brothers & Co

Recalled Item: BUSH'S BEST¿ Homestyle TANGY SAUCE WITH BACON & BROWN SUGAR Recalled by Bush...

The Issue: Discovered swollen cans

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 11, 2017· Bush Brothers & Co

Recalled Item: BUSH'S BEST¿ Original SEASONED WITH BACON & BROWN SUGAR BAKED Recalled by...

The Issue: Discovered swollen cans

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2017· New Century Snacks LLC

Recalled Item: Happy Belly Cranberry & Nuts Trail Mix - dried cranberries Recalled by New...

The Issue: Firm was notified by customer that the back panel (ingredients and nutrition...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2017· New Century Snacks LLC

Recalled Item: Happy Belly Deluxe Mixed Nuts - roasted and salted with sea salt. Cashews...

The Issue: Firm was notified by customer that the back panel (ingredients and nutrition...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Beckman Coulter Inc.

Recalled Item: iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100...

The Issue: iQ200 Series Urine Microscopy Analyzer may intermittently fail to read urine...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution - Premixed Dialysate for Hemodialysis with...

The Issue: Using different fluid formulations of NxStage PureFlow B Solution at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
DrugNovember 10, 2017· Baxter Healthcare Corporation

Recalled Item: Nexterone (amiodarone HCl) Premixed Injection Recalled by Baxter Healthcare...

The Issue: Presence of Particulate Matter:Particulate identified as polyethylene, the...

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

Class I — Serious Health HazardOngoing
Refund