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 2608126100 of 55,304 recalls

FoodOctober 4, 2018· Vosges Haut-Chocolat

Recalled Item: Caramels et Chocolats. Each retail tube contains four varieties on Recalled...

The Issue: Multi-pack product does not declare wheat on outer packaging, wheat is...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 4, 2018· Callie's Charleston Biscuits

Recalled Item: Callie's Charleston Biscuits COUTRY HAM BISCUITS Recalled by Callie's...

The Issue: The firm was notified by one of their vendors that the ham used in their...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Native Remedies VaricoGo Oral Spray Recalled by Silver Star Brands Due to...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Native Remedies EyeClear Pro Oral Spray Recalled by Silver Star Brands Due...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Native Remedies HypoSlim Oral Spray Recalled by Silver Star Brands Due to...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· Pfizer Inc.

Recalled Item: Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL...

The Issue: Correct Labeled Product Mispack: confirmed report involving a single unit of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Healthful Naturals DizziFree Oral Spray Recalled by Silver Star Brands Due...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Native Remedies VertiFree Oral Spray Recalled by Silver Star Brands Due to...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Healthful Naturals Leg Cramp Support Oral Spray Recalled by Silver Star...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: Amlodipine Besylate USP 10 mg Tablets Recalled by InvaGen Pharmaceuticals,...

The Issue: Subpotent Drug: One lot of product does not meet the product specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 3, 2018· Medtronic Inc.

Recalled Item: Medtronic MiniMed 630G 6025805-003_C Recalled by Medtronic Inc. Due to...

The Issue: Reports of occurrences in which insulin pumps with version 4.10 software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2018· GE Medical Systems, LLC

Recalled Item: SIGNA Architect system Product Usage: The Signa Architect system is Recalled...

The Issue: A small area on the bore surface, which is normally accessible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14ML/HR 2ML-30LO CPNB Recalled by Arrow International Inc...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare HeatWraps Menstrual a) b) Product Recalled by Pfizer Inc. Due to...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare Muscle Pain Therapy HeatWraps: a) b) Recalled by Pfizer Inc. Due...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare HEATWRAPS JOINT PAIN THERAPY Recalled by Pfizer Inc. Due to The...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14ML/HR CPNB Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14 ml/hr Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 5ML/H 6" CATH Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 5ML/H 6" DUAL CATHS Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing