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 15941–15960 of 55,304 recalls

DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Fulvestrant Injection 250 mg/5 mL (50 mg/mL) For Intramuscular Use Recalled...

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
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Zonisamide Capsules USP 50 mg 100 Capsules Rx Only NDC Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Naproxen Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Naproxen Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Zonisamide Capsules USP 100 mg Rx Only Manufactured by: Glenmark Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· DuPont Nutrition USA, Inc

Recalled Item: Avicel RC-591 NF (MCC/Carboxymethylcellulose Sodium) NF Recalled by DuPont...

The Issue: Microbial Contamination of Non-Sterile Product: Out-of-specification results...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 27, 2021· PTW NORTH AMERICA CORPORATION

Recalled Item: Software BeamAdjust version 2.2 Recalled by PTW NORTH AMERICA CORPORATION...

The Issue: When a measurement with a PTW detector array is performed with the software...

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

Class II — Potential Health HazardOngoing
DrugAugust 26, 2021· AVRIO HEALTH L.P

Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by AVRIO...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: 1.5T SIGNA HDxt MR System nuclear magnetic resonance imaging system Recalled...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Pioneer nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: Optima MR450w 1.5T nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Architect nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Creator Recalled by GE Healthcare, LLC Due to Under certain...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: Discovery MR750w 3.0T nuclear magnetic resonance imaging system Recalled by...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Voyager nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Artist nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: Discovery MR750 3.0T nuclear magnetic resonance imaging system Recalled by...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Premier nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· Atrium Medical Corporation

Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...

The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing