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 31413160 of 55,304 recalls

Medical DeviceMarch 11, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower Recalled by CareFusion...

The Issue: Due to a software bug, automated dispensing cabinet is unable to calculate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Revised C Reactive Protein (RCRP) Recalled by Siemens Healthcare...

The Issue: Incorrect software flagging may occur for the assay that may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID Recalled...

The Issue: Due to a software issue, when attempting to restock the automated dispensing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Medtronic Xomed, Inc.

Recalled Item: NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 Recalled by...

The Issue: Nerve Monitoring System with certain software versions has potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Philips North America Llc

Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for collimator to fall as a result of incorrect installation.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Maquet Cardiovascular, LLC

Recalled Item: Maquet VH-3010 Power Supply. Used to deliver power to the Recalled by Maquet...

The Issue: Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Philips North America Llc

Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for collimator to fall as a result of incorrect installation.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2025· Straumann USA LLC

Recalled Item: TLX/TLC SP Guided Implant Driver Recalled by Straumann USA LLC Due to The...

The Issue: The devices are missing the laser marked depth markings.

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

Class II — Potential Health HazardOngoing
DrugMarch 7, 2025· Direct Rx

Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Direct Rx

Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· ASEGUA THERAPEUTICS LLC

Recalled Item: Sofosbuvir and Velpatasvir Recalled by ASEGUA THERAPEUTICS LLC Due to...

The Issue: Defective Container: blister packs not properly sealed resulting in tablets...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Mylan Institutional, Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...

The Issue: Super-Potent Drug: Out of specification potency results were obtained.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Slate Run Pharmaceuticals

Recalled Item: Cinacalcet Hydrochloride Tablets 60 mg Recalled by Slate Run Pharmaceuticals...

The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Mylan Institutional, Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...

The Issue: Super-Potent Drug: Out of specification potency results were obtained.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Slate Run Pharmaceuticals

Recalled Item: Cinacalcet Hydrochloride Tablets 30 mg Recalled by Slate Run Pharmaceuticals...

The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 Recalled by Ethicon Endo Surgery,...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing