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 2630126320 of 55,304 recalls

FoodSeptember 12, 2018· Swire Coca Cola USA

Recalled Item: Caffeine-Free Barq s Root Beer 12 Pack Recalled by Swire Coca Cola USA Due...

The Issue: Recalling Caffeine-Free Barq s Root Beer 12 Pack due to mislabeling.

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

Class III — Low RiskOngoing
Refund
FoodSeptember 12, 2018· Sarap Asian Fusion

Recalled Item: Black Sesame White Chocolate (cookies) Recalled by Sarap Asian Fusion Due to...

The Issue: Undeclared wheat, soy lecithin, and milk

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2018· COCA COLA BOTTLING COMPAN

Recalled Item: NO SUGAR NO CALORIES Diet Coke 12 FL OZ (355 Recalled by COCA COLA BOTTLING...

The Issue: Product contains plastic material.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2018· COCA COLA BOTTLING COMPAN

Recalled Item: CAFFEINE FREE Diet Coke 12 FL OZ (355 ml) CONTAINS Recalled by COCA COLA...

The Issue: Product contains plastic material.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2018· Sarap Asian Fusion

Recalled Item: Ube Cookies & Cream (cookies) Recalled by Sarap Asian Fusion Due to...

The Issue: Undeclared wheat, soy lecithin, and milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 3000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Synthes (USA) Products LLC

Recalled Item: 3.0mm Headless Compression Screw Recalled by Synthes (USA) Products LLC Due...

The Issue: The product inside the package does not match the label. The product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Howmedica Osteonics Corp.

Recalled Item: Tritanium TL Steerable Inserter Recalled by Howmedica Osteonics Corp. Due to...

The Issue: The firm received complaints related to the locking mechanism on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· CMP Industries, Llc

Recalled Item: Technoflux IMPAK Resina lfquida acrilica elastic Curado-Calor Tipo 1...

The Issue: Foreign material in product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· CMP Industries, Llc

Recalled Item: IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1 Recalled by CMP...

The Issue: Foreign material in product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 2000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 500 mL - Product Usage: Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 1000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: PROCARE B20 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· TiSport, Llc

Recalled Item: TiLite X-Short anti-tip tubes Recalled by TiSport, Llc Due to The anti-tip...

The Issue: The anti-tip tubes potentially fail in certain situations and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B105/125 Patient Monitor. The device is a portable multiparameter unit...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B40i Patient Monitor and B40i Patient Monitor V3 The device Recalled by GE...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B20i Patient Monitor and B20i V2 Patient Monitor. The device Recalled by GE...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: PROCARE B40 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing