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. 1,958 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,958 in last 12 months

Showing 2786127880 of 30,032 recalls

Medical DeviceApril 12, 2013· Becton Dickinson & Co.

Recalled Item: BBL DrySlide Oxidase Kit Recalled by Becton Dickinson & Co. Due to In-vitro...

The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Becton Dickinson & Co.

Recalled Item: BBL DrySlide PYR Kit Recalled by Becton Dickinson & Co. Due to In-vitro...

The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Coloplast Manufacturing US, LLC

Recalled Item: Rostorelle L Recalled by Coloplast Manufacturing US, LLC Due to Mislabeling

The Issue: Coloplast is recalling one lot of Restorelle L prosthesis because it is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing