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. 1,137 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,137 in last 12 months

Showing 16201–16220 of 55,304 recalls

Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A399400A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A902616 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A300316A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A902416 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A942216 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A800360 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· Armstrong Medical Services Limited

Recalled Item: AMSORB PLUS PREFILLED G-CAN 1.0L Recalled by Armstrong Medical Services...

The Issue: Some devices may be associated with high and unexpected resistance to gas...

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

Class I — Serious Health HazardOngoing
DrugAugust 5, 2021· Hikma Pharmaceuticals USA Inc.

Recalled Item: Bleomycin for Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Labeling: Not elsewhere classified: Mislabeling

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

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2021· DuPont Nutrition USA, Inc

Recalled Item: Avicel Recalled by DuPont Nutrition USA, Inc Due to Out of specification...

The Issue: Out of specification results for conductivity.

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

Class III — Low RiskOngoing
Refund
FoodAugust 4, 2021· Molly and Me Pecans

Recalled Item: MOLLY & ME PECANS all natural PRALINE PECANS Recalled by Molly and Me Pecans...

The Issue: The firm was notified during an inspection by the State that the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2021· OLAM Edible Nuts-Blakely,GA

Recalled Item: Raw Shelled Peanuts Recalled by OLAM Edible Nuts-Blakely,GA Due to Firm was...

The Issue: Firm was notified of metal objects in the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 4, 2021· Abbott Molecular, Inc.

Recalled Item: Vysis CLL FISH Probe Kit with the following components: Vysis Recalled by...

The Issue: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Mac Medical Supply Co Inc

Recalled Item: Ultrasound Gel labeled under the following brand names: MediChoice...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System...

The Issue: Customers have reported an increased number of false positive SARS-CoV-2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Olympus Corporation of the Americas

Recalled Item: Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8 Recalled by...

The Issue: Packaging seal defect may allow a breach of the package sterile barrier and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Luminex Corporation

Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...

The Issue: There is potential for false positive results.

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

Class II — Potential Health HazardOngoing
DrugAugust 3, 2021· Teligent Pharma, Inc.

Recalled Item: Lidocaine Hydrochloride Topical Solution Recalled by Teligent Pharma, Inc....

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund