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. 1,973 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,973 in last 12 months

Showing 2602126040 of 30,032 recalls

Medical DeviceMarch 17, 2014· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-80. Product Usage: intended...

The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Philips Medical Systems, Inc.

Recalled Item: Digital Diagnost Recalled by Philips Medical Systems, Inc. Due to The...

The Issue: The footboard of Patient support for stitching can be fixed in upper...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· 3M Company - Health Care Business

Recalled Item: 3M" Steri-Vac" Gas Sterilizer/Aerators Recalled by 3M Company - Health Care...

The Issue: Recently, 3M received a single report of a potential exposure to Ethylene...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Remel Inc

Recalled Item: Oxoid Legionella Pneumo Groups 2-14 Recalled by Remel Inc Due to A reagent...

The Issue: A reagent contained within the product may return false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2014· Claymount Assembli

Recalled Item: The Claymount Harmony is a grid cabinet designed to accept Recalled by...

The Issue: Claymount Assemblies BV is recalling the Harmony2 model of Harmony Bucky...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2014· Claymount Assembli

Recalled Item: The Claymount Harmony is a grid cabinet designed to accept Recalled by...

The Issue: Harmony1 models of the Harmony Bucky is incorrectly labeled in that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...

The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The products are labeled as sterile but were not sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...

The Issue: The products are labeled as sterile but were not sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Bard Fixt Suture Braided Polyester Recalled by Teleflex Medical Due to...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Dekna-lok Recalled by Teleflex Medical Due to The product did not meet...

The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port  Long Length...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10/12 mm Weck¿ Vista" Optical Bladeless Laparoscopic Access Port Recalled...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Weck Vista Universal Laparoscopic Port Recalled by Teleflex Medical Due to...

The Issue: Complaints of leakage of insufflation gas through the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Nonabsorbable Surgical Suture Recalled by Teleflex Medical Due to Product...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing