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 4990149920 of 55,304 recalls

Medical DeviceAugust 1, 2013· Zimmer, Inc.

Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...

The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...

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

Class II — Potential Health HazardOngoing
DrugJuly 31, 2013· Actavis Inc

Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Actavis...

The Issue: Failed Dissolution Specifications: Dissolution test results at 8 hour...

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

Class III — Low RiskOngoing
Refund
FoodJuly 31, 2013· Les 3 Comtois

Recalled Item: Morbier Les 3 Comtois Recalled by Les 3 Comtois Due to Potential Listeria...

The Issue: FDA analysis of Morbier Semi-Soft Cheese (prior to entry) revealed the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 31, 2013· Leica Biosystems Newcastle Ltd.

Recalled Item: Leica BIOSYSTEMS Recalled by Leica Biosystems Newcastle Ltd. Due to The...

The Issue: The affected lots of the product may contain a contaminant of fungus that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Large Buttress Compression Nut For Blade Guide Sleeve TFN The Recalled by...

The Issue: The Large Buttress Compression Nut For Blade Guide Sleeve TFN was recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...

The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...

The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...

The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...

The Issue: Synthes became aware that during a procedure using the Matrix Threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Fujinon Inc

Recalled Item: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images...

The Issue: A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Edwards Lifesciences, LLC

Recalled Item: "***Flo Trac Sensor Model MHD85***" Sterile Recalled by Edwards...

The Issue: The Edwards Lifesciences FloTrac Sensor is being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Arrow International Inc

Recalled Item: Arrow International Recalled by Arrow International Inc Due to Arrow is...

The Issue: Arrow is recalling the product due to a labeling inconsistency. One portion...

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

Class II — Potential Health HazardOngoing
DrugJuly 30, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Belladonna Alkaloids with Phenobarbital Tablets Recalled by West-Ward...

The Issue: Presence of Foreign Substance: black specks comprised of degraded organic...

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

Class II — Potential Health HazardOngoing
Refund