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. 1,909 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,909 in last 12 months

Showing 3472134740 of 55,304 recalls

FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# CHUCK E CHEESE Pasteurized Recalled...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: WHOLE MILK CHEESE 8/6# ARREZZIO CLASSIC Recalled by Saputo Cheese USA, Inc....

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# ARREZZIO IMPERIAL Recalled by Saputo...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# CHEESECAKE FACTORY TCCFI Recalled by...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# DRAGONE Recalled by Saputo Cheese...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· NATURECOM INC

Recalled Item: DMAA (1 Recalled by NATURECOM INC Due to Naturecom dba NutriVitaShop is...

The Issue: Naturecom dba NutriVitaShop is recalling DMAA net weight 500 g because there...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: WHOLE MILK CHEESE 8/6# MAGIC MOZZI Recalled by Saputo Cheese USA, Inc. Due...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Green Dirt Farm, LLC

Recalled Item: Green Dirt Farm "Ruby" blended milk cheese packaged in cases of 6 Recalled...

The Issue: Product is contaminated with Staphylococcus aureus exceeding action limit of...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA SUPREME 8/6# CONTADINO Recalled by Saputo Cheese USA, Inc. Due to...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2016· To Your Heart's Content

Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...

The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2016· Les Emballages Knowlton Inc.

Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...

The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.

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

Class III — Low RiskOngoing
Refund
DrugNovember 22, 2016· Pfizer Inc.

Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....

The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Optimus Fixed Awl Recalled by Amendia, Inc Due to Complaints that the tip of...

The Issue: Complaints that the tip of the awl broke after impaction during surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Teleflex Medical

Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...

The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...

The Issue: There is a problem with the mating feature between the plate and screw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Scope Power Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is providing a new installation of the Residual Current Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...

The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Interventional Spine Inc

Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...

The Issue: During implantation, the proximal end of the device could separate if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Perspective Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is providing a new installation of the Residual Current Monitor...

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

Class II — Potential Health HazardOngoing