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. 1,097 recalls have been distributed to Illinois in the last 12 months.
Showing 18601–18620 of 55,304 recalls
Recalled Item: Mesalamine Delayed-Release Tablets Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Dissolution Specifications: Out-of-specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Art Of Tea - Feel Better tea Recalled by Art Of Tea Due to Potential...
The Issue: Firm was notified by supplier of Elder Berries of a recall due to potential...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pacific Jade Indian Curry Sauce Starter With Fenugreek and Cardamom Recalled...
The Issue: Product declared on shipping case does not match the inner packaged product....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G Recalled...
The Issue: The manufacturer has determined that with certain uncommon workflows there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAC VU360 Recalled by GE Healthcare, LLC Due to Incorrect patient...
The Issue: Incorrect patient identification and/or patient demographic errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI TROCAR KIT 23G S - Product Usage: for use Recalled by Mani, Inc. -...
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI Infusion Cannula 23G S - Product Usage: for use Recalled by Mani, Inc....
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg Recalled by...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroex (chlorhexidine gluconate) Oral Rinse Recalled by Sunstar Americas,...
The Issue: Microbial Contamination of Non-sterile Products: contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Ascent...
The Issue: Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone Bitartrate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Orally Disintegrating Tablets Recalled by Jubilant Cadista...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults. When a 2D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for Recalled by Becton...
The Issue: Product shelf cartons incorrectly labeled as products intended for the Latin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) PRO+ System. With the following model numbers: a. Recalled by...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: ION Fully Articulating Catheter Recalled by Intuitive Surgical,...
The Issue: The distal tip ring of the fully articulating catheter may become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Pump - Product Usage: indicated for male patients suffering Recalled...
The Issue: Potential increased occurrence of pump fracture over the lifetime of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in Recalled by...
The Issue: The firm has become aware of nine reports by a single customer that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mako Integrated Cutting System (MICS) Handpiece Recalled by Mako Surgical...
The Issue: Stryker has discovered a characterization issue associated with the Mako...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.