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. 1,974 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,974 in last 12 months

Showing 2588125900 of 30,032 recalls

Medical DeviceApril 16, 2014· Baxter Corporation Englewood

Recalled Item: RAPIDFILL Syringe Strip Recalled by Baxter Corporation Englewood Due to...

The Issue: Possible breach in sterile barrier for inner and outer bags of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Maquet Medical Systems USA

Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...

The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Sakura Finetek USA Inc

Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...

The Issue: This Lot has variations in melting temperature.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· HeartWare Inc

Recalled Item: HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) -...

The Issue: Patients and caregivers are instructed that if a battery does not provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Synthes, Inc.

Recalled Item: DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies...

The Issue: DePuy Synthes is initiating a recall of certain lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 16, 2014· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...

The Issue: Test Strips may report an inaccurately low INR result. Several patients had...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 15, 2014· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Infant Nasal CPAP (continuous positive airway pressure) Prong Recalled by...

The Issue: The Infant Nasal CPAP Prong has the potential to detach from the Nasal...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 15, 2014· Brainlab AG

Recalled Item: ExacTrac 5.5 Recalled by Brainlab AG Due to When using a specific plan...

The Issue: When using a specific plan update workflow in combination with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Handicare USA, Inc.

Recalled Item: ReTurn 7500/7500 Aid Recalled by Handicare USA, Inc. Due to During the...

The Issue: During the period of April 2009  May 2011, Handicare AB used a wing handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Healthcare Diagnostics Vista Air Compressor. Vista AirCompressor...

The Issue: A small number of Vista Air Compressors were miswired, which if installed...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Microline Surgical

Recalled Item: Microline Renew Fenestrated Control Tip Grasper Recalled by Microline...

The Issue: Grasper jaw may break when force is applied to the jaw

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Ivoclar Vivadent, Inc.

Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...

The Issue: A stock check revealed broken glass fibers between the connector and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...

The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Arrow International Inc

Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...

The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...

The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing