State

Illinois product recalls

20,371 recalls have nationwide distribution and so reach Illinois. 0 additional recalls listed Illinois specifically in their distribution scope.

About recalls in Illinois

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Illinois consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

16026–16050 of 20371

ModerateFDA (Devices)·Z-1539-2022·2022-08-24
Poligrip Denture Adhesive Products Recalled for Improper Storage Conditions
Family Dollar Stores recalls multiple Poligrip denture adhesive products due to improper storage outside temperature-controlled areas. Affected products were sold between May 1 and June 10, 2022.
Product
POLIGRIP ADH CREAM FREE 2.4OZ, SKU 900334 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ, SKU 900723 SUPER POLIGRIP ADH CREAM .75OZ, SKU 900085
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1343-2022·2022-08-24
Rifampin Capsules Recalled Due to Manufacturing Control Deviation
Lupin Pharmaceuticals is recalling Rifampin 150 mg capsules (lot #A200170) nationwide due to a Current Good Manufacturing Practice deviation with an out-of-specification impurity detected during manufacturing.
Product
RIFAMPIN — RIFAMPIN (RIFAMPIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1535-2022·2022-08-24
Travel Kit Toothbrush and Toothpaste Recalled Due to Improper Storage
Family Dollar is recalling approximately 1,555 travel kit toothbrush and toothpaste pouches that were stored in non-temperature-controlled areas. Products sold between May 1 and June 10, 2022 are affected.
Product
TRVL KIT TOTHBRSH CAP PASTE IN POUCH 1CT, SKU 900737
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1547-2022·2022-08-24
KY Jelly Lubricant Recalled for Improper Storage Conditions
KY Jelly Lubricant 2 FL OZ (SKU 901443) distributed at Family Dollar stores was not stored in temperature-controlled areas. Consumers should discontinue use of product purchased between May–June 2022.
Product
KY JELLY LUBRICANT 2 FL OZ, SKU 901443
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1542-2022·2022-08-24
At-home marijuana test strips recalled for improper storage
Family Dollar is recalling at-home marijuana test strips (SKU 900752) that were stored outside temperature-controlled areas. Improper storage may affect test accuracy.
Product
AT HOME MARIJUANA TEST STRIP, SKU 900752
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1536-2022·2022-08-24
CURAD Waterproof Bandages Recalled for Improper Storage
Family Dollar is recalling CURAD waterproof bandages due to improper storage outside temperature-controlled conditions. The recall affects approximately 419 units sold nationwide between May 1 and June 10, 2022.
Product
CURAD STRNG WATRPRF STRIP 1IN 20CT, SKU
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22202·2022-08-18
Hard Rock Cafe Children's Hooded Sweatshirts Recalled for Strangulation Hazard
Hard Rock Cafe is recalling about 1,550 children's hooded sweatshirts with drawstrings in the hood that can become entangled or caught on objects, posing a strangulation hazard to children. No injuries have been reported.
Product
Hard Rock Cafe Children's Hooded Sweatshirts
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22201·2022-08-18
ASUS ROG Maximus Z690 Hero Motherboards Recalled for Fire and Burn Hazards
ASUS Computer International is recalling about 10,000 ASUS ROG Maximus Z690 Hero motherboards because a capacitor installed in reverse position can cause short circuits, overheating, or melting. ASUS has received 10 reports of overheating and melting, though no injuries have been reported.
Product
ASUS ROG Maximus Z690 Hero Motherboards
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1399-2022·2022-08-17
FDA Recalls 3.95 Million Viral Transport Containers Distributed Without Clearance
The FDA recalled 3.95 million viral transport containers distributed without FDA clearance and in violation of established guidance. The containers were distributed worldwide, including to facilities in California, Florida, Illinois, and New York.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1398-2022·2022-08-17
FDA Recalls Viral Transport Containers Distributed Without Clearance
FDA recalls approximately 8.7 million viral transport containers that were distributed without regulatory clearance and without complying with FDA guidance for proper viral transport specifications.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1400-2022·2022-08-17
Viral Transport Container Distributed Without FDA Clearance or Guidance Compliance
Haimen Shengbang Laboratory Equipment recalled 100,000 viral transport containers distributed without FDA clearance and outside FDA guidance, affecting facilities in California, Florida, Illinois, New York, and China.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1332-2022·2022-08-17
Fentanyl Citrate IV Bags Recalled Due to Sterility Assurance Failure
SterRx is recalling 360 bags of fentanyl citrate IV medication due to lack of assurance of sterility. No illnesses have been reported.
Product
fentaNYL Citrate in 0.9% Sodium Chloride, 2.5 mg per 250 mL, (10 mcg per mL) IV bags, Rx Only, SterRx, 141 Idaho Avenue, Plattsburgh, NY 12903, NDC 70324-327-02.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2022·2022-08-17
Lithotripsy Generator Recall Due to Mis-Wired Component Affecting System Reliability
Olympus Corporation recalls 2 units of the ShockPulse-SE Lithotripsy Generator due to a mis-wired component that causes improper power supply noise and EMC non-compliance, potentially affecting device reliability and treatment delivery.
Product
ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1540-2022·2022-08-17
Aivia Whey Protein Chocolate Recalled for Undeclared Milk Allergen
Nature's Sunshine Products is recalling Aivia Whey Protein+ Power Herbs Chocolate because the label declares whey but fails to declare milk. Approximately 2,747 bags were distributed nationwide.
Product
Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904 22711 8 Label is read in parts: "***INGREDIENTS: Whey Isolate, Whey Concentration***".
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1509-2022·2022-08-17
MetaFix hip stem mislabeled with wrong size and batch information
A Corin MetaFix hip stem (size 7 collarless) was incorrectly labeled as a size 3 collared stem with wrong batch information. The labeling error creates risk during surgical implantation.
Product
Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2022·2022-08-17
Xhibit Telemetry Receiver Model 96280 alarm escalation software defect
Xhibit Telemetry Receiver Model 96280 units fail to escalate critical alarms after approximately 25 days of continuous use, including signal loss, low battery, and SpO2 sensor issues. Caregivers may not be aware of device failures.
Product
Xhibit Telemetry Receiver, Model: 96280
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1310-2022·2022-08-17
Lorazepam Injection Recalled for Out-of-Specification Impurities and Degradation
Hikma Pharmaceuticals is recalling 82,700 vials of Lorazepam Injection due to failed quality specifications for impurities and degradation. Lot #070096 (expired July 2023) was distributed nationwide.
Product
LORAZEPAM — LORAZEPAM (LORAZEPAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1506-2022·2022-08-17
HAIOU Retractable Safety Syringes Recalled for Needle Detachment Risk
HAIOU retractable safety syringes are recalled due to reports of needle detachment from the syringe after injection and failure to retract, increasing needle stick injury risk. Approximately 4.05 million units are affected.
Product
HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G x 1-inch needle} 200 pieces/box. Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-25G25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1328-2022·2022-08-17
Difluprednate eye drops recalled for defective container closure affecting sterility
Cipla is recalling Difluprednate ophthalmic emulsion nationwide due to defective container closures that compromise sterility assurance. Patients using the affected lot should discontinue use and contact their healthcare provider.
Product
DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2022·2022-08-17
Roche cobas e801 Analyzer Recall: Software Defect Affects Test Results
Roche is recalling approximately 965 cobas e801 Immunoassay Analyzers nationwide due to a software issue that impacts Pre-Wash test signals and results for six diagnostic assays. No injuries or illnesses have been reported.
Product
cobas e801 Immunoassay Analyzer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1330-2022·2022-08-17
Prednisone Tablets Recalled for Contamination With Wrong-Strength Tablets
Strides Pharma is recalling Prednisone 20 mg tablets due to contamination with 2.5 mg tablets. No illnesses have been reported, but patients may receive incorrect doses.
Product
PREDNISONE — PREDNISONE (PREDNISONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1315-2022·2022-08-17
Eye-stream Eye Wash Solution Recalled for Improper Storage
Mckesson Medical-Surgical has recalled Eye-stream eye wash solution nationwide due to storage conditions outside drug label specifications.
Product
Eye-stream, eye wash solution, sterile, 4 FL OZ (118 mL) bottle per box, Alcon, NDC 0065-0530-04.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1313-2022·2022-08-17
Eye Drops Recalled Due to Improper Storage Violating Manufacturing Standards
Naphcon A eye drops are being recalled nationwide because products were stored outside label specifications, violating Current Good Manufacturing Practice (CGMP) standards.
Product
NAPHCON A — NAPHCON A (NAPHAZOLINE HYDROCHLORIDE AND PHENIRAMINE MALEATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1311-2022·2022-08-17
Triple Antibiotic Ointment Recalled Due to Improper Storage
McKesson Medical-Surgical Inc. is recalling Triple Antibiotic Ointment due to storage deviations that violated drug label specifications and current good manufacturing practices.
Product
Triple Antibiotic Ointment, Bacitracin zinc, Neomycin sulfate, Polymixin B sulfate, First Aid Antibiotic, Triple Antibiotic Ointment, 144 packets per box, Net wt. per packet 0.5 g, Honeywell Safety Products, NDC 0498-0750-36.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1507-2022·2022-08-17
Haiou Needle Retractable Safety Syringe recalls due to needle detachment risk
Approximately 7,218,000 Haiou Needle Retractable Safety Syringes are being recalled due to needle detachment and retracting mechanism failures that increase needlestick injury risk. The affected product was distributed in California.
Product
Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 (0.6x25mm). 200pcs/Box Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-23G25
Category
Medical Device
Distribution
Distributed nationwide