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. 2,733 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,733 in last 12 months

Showing 2900129020 of 55,304 recalls

Medical DeviceMarch 14, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect simply InterActive Implant Recalled by Implant Direct Sybron...

The Issue: The cap on the vial might be labeled with the incorrect part number but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart (HS1) Onsite/Home AED Recalled by Philips Electronics...

The Issue: An issue with one of the electric components (a resistor) could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Invivo Corporation

Recalled Item: PHILIPS Xper Flex Cardio Physiomonitoring System Recalled by Invivo...

The Issue: The real-time numeric value for ventricular end-diastolic pressure (EDP)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision Recalled by...

The Issue: After continuous operation for more than one and a half days, the image on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Polymer Technology Systems, Inc.

Recalled Item: PTS Panels¿ CHOL+GLU Test Strips () Recalled by Polymer Technology Systems,...

The Issue: Potential for loss of activity of the glucose analyte (under-recovery) prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Accelerate Diagnostics Inc

Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...

The Issue: The kits may produce an elevated rate of false positive calls for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· BioFire Diagnostics, LLC

Recalled Item: FilmArray BCID Panel (Blood Culture Identification Panel) Recalled by...

The Issue: There is an increased risk of false positive Proteus results when the...

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

Class II — Potential Health HazardOngoing
FoodMarch 13, 2018· Mondelez Global Llc

Recalled Item: Sour Patch Kids Recalled by Mondelez Global Llc Due to Mondelez Global LLC...

The Issue: Mondelez Global LLC is initiating a recall because remnants of a half peanut...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 13, 2018· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...

The Issue: The firm received complaints of drill bits breaking during use with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2018· Keystone Dental Inc

Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...

The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Ohio Medical Corporation

Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...

The Issue: Final quality control testing was not completed before the devices were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults...

The Issue: After two and a half years, the battery fuel gauge may indicate a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· CooperSurgical, Inc.

Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...

The Issue: Products have been packaged with the wrong Trocar length type.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker GmbH

Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...

The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C3 Ventilator Unit Intended to provide ventilator support to adults...

The Issue: After two and a half years, the battery fuel gauge may indicate a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...

The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2018· Akorn, Inc.

Recalled Item: Triamcinolone Acetonide Lotion Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class III — Low RiskOngoing
Refund
DrugMarch 9, 2018· Alva-Amco Pharmacal Companies., Inc.

Recalled Item: Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal Recalled by...

The Issue: Subpotent Drug: The product has failed to maintain its label claim of coal...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 9, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C3 Ventilator Unit Product Usage: The HAMILTON-C3 ventilator is...

The Issue: An out of specification component on the control board may cause the...

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

Class II — Potential Health HazardOngoing