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. 2,059 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,059 in last 12 months

Showing 1640116420 of 30,032 recalls

Medical DeviceJuly 3, 2018· Alden Optical

Recalled Item: Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a Recalled by...

The Issue: Vials labeled for the prescriptions contained incorrect lenses

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2018· Alden Optical

Recalled Item: Zen RC Toric-Gas permeable contact lenses for Daily Wear in Recalled by...

The Issue: Vials labeled for the prescriptions contained incorrect lenses

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2018· Arrow International Inc

Recalled Item: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...

The Issue: One lot of product is from product code AK-22502 so it contains a 2-lumen, 5...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· ConvaTec, Inc

Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...

The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Radiometer America Inc

Recalled Item: Product: ABL800 FLEX with Crea. The ABL800 with Crea is Recalled by...

The Issue: From three incidents in Denmark and Sweden, comparison studies on patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Cypress Medical Products LLC

Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...

The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Hudson Scientific LLC

Recalled Item: iTOVi Tracker/Scanner Recalled by Hudson Scientific LLC Due to The device...

The Issue: The device and its accessories may not have been manufactured according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Water Pik, Inc.

Recalled Item: Waterpik Sonic-Fusion Professional Recalled by Water Pik, Inc. Due to...

The Issue: Charging base may overheat with localized melting and sparking, possibly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Luminex Corporation

Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...

The Issue: An incorrect control board and firmware installed in some of the Hand Held...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Connect (SMN 11069018). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution Recalled by...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Pure Rayz Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not receive...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Baby Quasar Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D V Recalled by Siemens Medical Solutions USA, Inc Due to In rare cases of...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing