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. 1,048 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,048 in last 12 months

Showing 36481–36500 of 55,304 recalls

Medical DeviceJuly 1, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...

The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Mentor Texas, LP.

Recalled Item: Mentor MemoryGel Breast Implant Recalled by Mentor Texas, LP. Due to The box...

The Issue: The box of 300cc MemoryGel Breast Implant was labeled with null...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Sysmex America Inc

Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...

The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...

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

Class II — Potential Health HazardOngoing
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Strawberry Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Watermelon Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Original Lemonade Recalled by Coca-Cola Company (The) Due to Foreign...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Blackberry Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2016· Mister Cookie Face Corporation

Recalled Item: Sundae Shoppe Novelty Ice Cream Dipped "Variety"cones Recalled by Mister...

The Issue: Sundae Shoppe Novelty Ice Cream Dipped "Variety" Ice Cream Cones are being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Gmbh

Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...

The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· C.R. Bard, Inc.

Recalled Item: Medivance ArcticGel Neonatal Pad The pad is designed to fit Recalled by C.R....

The Issue: An internal review of an available product found that the Information For...

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

Class III — Low RiskOngoing
DrugJune 30, 2016· Actavis Inc

Recalled Item: Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc Due to...

The Issue: Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection Recalled by...

The Issue: Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· C.R. Bard, Inc.

Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem

The Issue: Labeling problem

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

Class III — Low RiskOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing