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. 2,959 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,959 in last 12 months

Showing 28812900 of 55,304 recalls

Medical DeviceApril 14, 2025· Augmedics Ltd.

Recalled Item: Augmedics Perc Pin Adaptor Recalled by Augmedics Ltd. Due to The perc pin...

The Issue: The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2025· Microtek Medical, Inc.

Recalled Item: Microtek Patient Drape ECOLAB AP6MMN Patient Drape Recalled by Microtek...

The Issue: Due to non-sterile products being labeled as sterile

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

Class II — Potential Health HazardOngoing
FoodApril 12, 2025· Dianne's Fine Desserts

Recalled Item: Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled:...

The Issue: Contains undeclared allergens (almonds).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 11, 2025· Medical Depot Inc.

Recalled Item: iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Recalled by Medical...

The Issue: Potential for DC Power Supply housing to become hot to the touch and deform...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2025· LeMaitre Vascular, Inc.

Recalled Item: Pruitt Occlusion Catheter. Catalog Numbers: 2103-36 Recalled by LeMaitre...

The Issue: During internal product testing, it was observed that some packages to have...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2025· LeMaitre Vascular, Inc.

Recalled Item: TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34...

The Issue: During internal product testing, it was observed that some packages to have...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2025· Nipro Renal Soultions USA, Corporation

Recalled Item: MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X)...

The Issue: Potential for the presence of visible foreign matter.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2025· LeMaitre Vascular, Inc.

Recalled Item: Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09 Recalled by...

The Issue: During internal product testing, it was observed that some packages to have...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Craniotomy Kit Recalled by Integra LifeSciences Corp. (NeuroSciences)...

The Issue: Inadequate weld that can potentially cause the product to disassemble.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Disposable Perforator Recalled by Integra LifeSciences Corp....

The Issue: Inadequate weld that can potentially cause the product to disassemble.

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

Class I — Serious Health HazardOngoing
DrugApril 10, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2025· Lupin Pharmaceuticals Inc.

Recalled Item: clomiPRAMINE hydrochloride Capsules USP Recalled by Lupin Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: an out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2025· Eugia US LLC

Recalled Item: Testosterone Cypionate Injection Recalled by Eugia US LLC Due to cGMP:...

The Issue: cGMP: complaints of crystals not redissolving into solution after warming...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 10, 2025· 3M Company

Recalled Item: 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355 Recalled...

The Issue: Field action to clarify the flow rates and inlet fluid temperatures, along...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 10, 2025· Vyaire Medical

Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...

The Issue: Adapters may disconnect during setup or while in use, potentially...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 10, 2025· Contec Medical Systems Co., Ltd.

Recalled Item: CMS8000 Patient Monitor Recalled by Contec Medical Systems Co., Ltd. Due to...

The Issue: Patient monitor has nine identified cybersecurity vulnerabilities.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2025· Vyaire Medical

Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...

The Issue: Adapters may disconnect during setup or while in use, potentially...

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

Class I — Serious Health HazardOngoing