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. 1,828 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,828 in last 12 months

Showing 5050150520 of 55,304 recalls

Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597604110 Articular Surface AC ART SURF 56/STRIPED GRN 10 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597001131 Femur CR PRC SURF HDN FEM CO-NID AML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Infusor SV and LV Elastomeric Infusion Devices. Indicated...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Medtronic is recalling...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Multiday lnfusor Recalled by Baxter Healthcare Corp. Due to Due...

The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Basal/Bolus Infusor. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BBL Brucella Laked Blood Agar with Kanamycin and Vancomycin (KV) Recalled by...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375...

The Issue: Ortho Clinical Diagnostics is recalling CM/RT wear pads which are a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BBL Campylobacter CSM Agar (Charcoal-Based Selective Medium) Recalled by...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL BBE // CDC Anaerobe Laked Sheep Blood Agar with KV Recalled by Becton...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL Anaerobe CNA Agar with 5% Sheep Blood // Recalled by Becton Dickinson...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL Schaedler K-V Agar with 5% Sheep Blood Recalled by Becton Dickinson &...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin (KV)...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Endogastric Solutions Inc

Recalled Item: EndoGastric Solutions EsophyX2 Device with Serosa Fastener and Accessories....

The Issue: Endogastric Solutions, Inc. has received a limited number of reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Carestream Health, Inc.

Recalled Item: Carestream DRX-Revolution Mobile X-ray System. Produces radiographic images....

The Issue: Carestream Health Inc. is recalling the power plug on their DRX-Revolution...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL BCYE Selective Agar with PAV Recalled by Becton Dickinson & Co. Due...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing