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 2670126720 of 55,304 recalls

Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite 25 GA Vit Cutter Recalled by Bausch & Lomb Inc...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2018· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Doxycycline Hyclate USP Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp....

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2018· Natures Bounty Inc

Recalled Item: BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH...

The Issue: High level of microcystin observed in the product.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2018· Graeters Manufacturing Company

Recalled Item: Graeter's HANDCRAFTED French Pot ICE CREAM Recalled by Graeters...

The Issue: Product is labeled as gluten free, however, it contains wheat.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect simply RePlant Implant Recalled by Implant Direct Sybron...

The Issue: The incorrect device was packaged in the vial.

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2018· Teva Pharmaceuticals USA

Recalled Item: Paliperidone Extended Release Tablets 9 mg Recalled by Teva Pharmaceuticals...

The Issue: Defective Delivery System: There is a potential for some tablets to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2018· Teva Pharmaceuticals USA

Recalled Item: Metformin Hydrochloride Extended Release Tablets Recalled by Teva...

The Issue: Defective Delivery System: There is a potential for some tablets to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2018· Teva Pharmaceuticals USA

Recalled Item: Paliperidone Extended Release Tablets 3 mg Recalled by Teva Pharmaceuticals...

The Issue: Defective Delivery System: There is a potential for some tablets to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2018· Teva Pharmaceuticals USA

Recalled Item: Fortamet (metformin HCl) extended release tablets Recalled by Teva...

The Issue: Defective Delivery System: There is a potential for some tablets to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2018· Teva Pharmaceuticals USA

Recalled Item: Metformin Hydrochloride Extended Release Tablets 1000 mg Recalled by Teva...

The Issue: Defective Delivery System: There is a potential for some tablets to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2018· Teva Pharmaceuticals USA

Recalled Item: PIO&METFORMIN 15/1000 mg Tab 1 (Pioglitazone and Metformin XT) tablets...

The Issue: Defective Delivery System: There is a potential for some tablets to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2018· Teva Pharmaceuticals USA

Recalled Item: Metformin Hydrochloride Extended Release Tablets 1000 mg Recalled by Teva...

The Issue: Defective Delivery System: There is a potential for some tablets to be...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 6, 2018· Country Favor Inc.

Recalled Item: BEST TASTE BRAND SNACK GINGER SLICED Recalled by Country Favor Inc. Due to...

The Issue: Product contains high levels of undeclared sulfites.

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

Class I — Serious Health HazardOngoing
Refund