Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,457 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,457 in last 12 months

Showing 2532125340 of 27,373 recalls

Medical DeviceApril 15, 2013· Hill-Rom, Inc.

Recalled Item: Hill-Rom 1000 Bed Recalled by Hill-Rom, Inc. Due to Complaints have been...

The Issue: Complaints have been reported for brakes disengaging when the bed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle InsuLinx Blood Glucose Monitoring System: For In Vitro Diagnostic...

The Issue: AT rare, extremely high glucose levels (1024 mg/dL and above), the FreeStyle...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 15, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray systems Product Usage: The Brilliance CT 64...

The Issue: Philips Healthcare received reports from the field that certain Brilliance...

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· 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· 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· 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· Ethicon Endo-Surgery Inc

Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...

The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...

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· Ethicon Endo-Surgery Inc

Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex...

The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Ethicon Endo-Surgery Inc

Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...

The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...

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· Paa Laboratories Inc

Recalled Item: Various types of Fetal Bovine Serum Bovine sourced Animal Sera Recalled by...

The Issue: Current product labeling band data sheets state that FBS Pharma Grade and...

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