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. 2,641 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,641 in last 12 months

Showing 5420154220 of 55,304 recalls

FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: Kerry Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 1, 2012· I-Flow LLC

Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...

The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· I-Flow LLC

Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...

The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Advanced Sterilization Products

Recalled Item: CIDEX OPA Recalled by Advanced Sterilization Products Due to The recall was...

The Issue: The recall was initiated because Advanced Sterilization Products has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...

The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...

The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that the outer carton label of this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 8.25 (209.6 mm) 0.5mm Tips Recalled by PSC Industries Inc...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T5 Hytrel Zipper Toga. Product Usage: The togas are intended Recalled by...

The Issue: The clear tape, that is intended to aid in the prevention of patients fluids...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4-Hytrel Zipper Toga Product Usage - The togas are intended Recalled by...

The Issue: The clear tape, that is intended to aid in the prevention of patients...

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

Class II — Potential Health HazardOngoing
DrugMay 31, 2012· Bayer HealthCare Pharmaceuticals Inc.

Recalled Item: Leukine sargramostim 5 x 500 mcg/mL vial Recalled by Bayer HealthCare...

The Issue: Impurities/Degradation Products: A confirmed out of specification result for...

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

Class III — Low RiskOngoing
Refund
FoodMay 31, 2012· The Broaster Company, LLC

Recalled Item: Broaster Fish Coating Recalled by The Broaster Company, LLC Due to...

The Issue: The Broaster Company, LLC is recalling three lots of Broaster Fish Coating...

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

Class II — Potential Health HazardOngoing
Refund