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. 2,730 recalls have been distributed to Illinois in the last 12 months.
Showing 31921–31940 of 55,304 recalls
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....
The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....
The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....
The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Visualase(R) Cooled Laser Applicator System (VCLAS) 15MM TIP...
The Issue: Medtronic has become aware that the VCLAS 15MM TIP cap, also to as Tuohy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal(R) Dolphin Inflation Device Recalled by DeRoyal Industries Inc Due...
The Issue: Lack of sterility assurance. There is a defect in the primary packaging of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NasalCrom (cromolyn sodium) Nasal Spray Recalled by Bausch & Lomb, Inc. Due...
The Issue: CGMP Deviations: Possibility of the presence of microbial contamination in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIRDS EYE CHILIES MJG # 8178 Recalled by Morris J. Golombeck, Inc. Due to...
The Issue: Product may contain peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis Recalled by Siemens Medical Solutions USA, Inc Due to Potential...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.Zen Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid...
The Issue: Potential for flouroscopially visible marker band at the tip of the Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliquisTablets 5mg Recalled by Bristol-myers Squibb Company Due to Labeling:...
The Issue: Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.