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 4778147800 of 55,304 recalls

Medical DeviceDecember 13, 2013· Highland Metals, Inc.

Recalled Item: SuperElastic Regular force NiTi lower or upper Natural arches. 0.14 Recalled...

The Issue: Labeling issue: Product labeled as "Upper" may contain "Lower" archwires...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2013· Highland Metals, Inc.

Recalled Item: SuperElastic Regular force NiTi lower or upper Natural arches. 0.16 Recalled...

The Issue: Labeling issue: Product labeled as "Upper" may contain "Lower" archwires...

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

Class II — Potential Health HazardOngoing
DrugDecember 12, 2013· Hospira Inc.

Recalled Item: Propofol Injectible Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Glass defect located on the interior neck of...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 12, 2013· Bee International, Inc.

Recalled Item: Candy Sweet Spots Recalled by Bee International, Inc. Due to Undeclared Egg

The Issue: Bee International is recalling Sweet Spots Candy because it has undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 12, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...

The Issue: Sterility of medical devices intended for use in surgical procedures may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· King Systems Corp.

Recalled Item: King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is Recalled...

The Issue: On December 13, 2012, King Systems initiated a voluntary recall of one (1)...

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

Class II — Potential Health HazardOngoing
DrugDecember 11, 2013· KVK-Tech, Inc.

Recalled Item: HydrOXYzine HCI Tablets USP 10 mg Recalled by KVK-Tech, Inc. Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an Active...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 11, 2013· KVK-Tech, Inc.

Recalled Item: HydrOXYzine HCI Tablets USP 25 mg Recalled by KVK-Tech, Inc. Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an Active...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 11, 2013· KVK-Tech, Inc.

Recalled Item: HydrOXYzine HCI Tablets USP 50 mg Recalled by KVK-Tech, Inc. Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an Active...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 11, 2013· Blooming Import Inc.

Recalled Item: GOLDEN LION brand DRIED ZIZIPHUS JUJUBA MILL (DRIED DATES) Recalled by...

The Issue: The product contained undeclared sulfites (1519 ppm) based on sampling and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 11, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2013· AdvanDx, Inc.

Recalled Item: AdvanDx Gram-Negative QuickFISH BC. In-Vitro Diagnostic for the...

The Issue: Kits incompatible with certain fluorescence microscope light sources

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

Class III — Low RiskOngoing
DrugDecember 10, 2013· Slim Beauty USA

Recalled Item: Magic Slim capsules (Ling Zhi Recalled by Slim Beauty USA Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund