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. 1,930 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,930 in last 12 months

Showing 3164131660 of 55,304 recalls

FoodJune 13, 2017· Channel Fish Processing Co. Inc

Recalled Item: Pacific Dynasty - Raw Breaded Cod Square 4 OZ - NET WT. 10 LBS (4.54 KG)...

The Issue: Products recalled due to undeclared allergen -milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 13, 2017· Channel Fish Processing Co. Inc

Recalled Item: Winsor Bay- Raw Oriental Breaded Fish Portions - 4 oz. Recalled by Channel...

The Issue: Products recalled due to undeclared allergen -milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 12, 2017· Zimmer Biomet, Inc.

Recalled Item: DRILL BIT MINI QUICK CONNECT 1.0MM Recalled by Zimmer Biomet, Inc. Due to A...

The Issue: A raw material anomaly was discovered in four lots of raw material and has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· CareFusion 303, Inc.

Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to BD initiated the...

The Issue: BD initiated the recall of Alaris PC unit model 8015 after the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Invuity, Inc.

Recalled Item: INVUITY(R) PhotonBlade(TM) Recalled by Invuity, Inc. Due to A small number...

The Issue: A small number of customer observations were recently received which related...

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

Class II — Potential Health HazardOngoing
DrugJune 12, 2017· Vi-Jon, Inc.

Recalled Item: Magnesium Citrate Saline Laxative Cherry Flavored Recalled by Vi-Jon, Inc....

The Issue: Presence of foreign substance: glass particle

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor...

The Issue: Superpotent Drug: high out-of-specification result for magnesium.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Recalled by Roche...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Recalled by...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe Recalled by Natus Neurology Inc...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 3 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 5 MHz Vascular Probe Recalled by Natus Neurology Inc Due to...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Sorin Group USA, Inc.

Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...

The Issue: Identification of excess plastic on the tip of the cannula.

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

Class II — Potential Health HazardOngoing