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. 907 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
907 in last 12 months

Showing 44781–44800 of 48,330 recalls

Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight2 Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT gamma camera for Emission Computed Tomography Recalled by...

The Issue: Philips has received one report from the field that there was an unexpected...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Leibel-Flarsheim Company LLC

Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...

The Issue: A complaint was received in which a hospital physicist indicated the dosage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2013· Embla System Llc

Recalled Item: embla Embletta Gold (It functions as a Polysomnography Recorder and Recalled...

The Issue: Calibration error for Embla Embletta Gold units calibrated through service...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2013· Insight Instruments, Inc.

Recalled Item: Cornea Coat Recalled by Insight Instruments, Inc. Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Fisher & Paykel Healthcare ICON CPAP (continuous positive airway pressure)....

The Issue: Fisher and Paykel Healthcare is recalling the ICON CPAP units because there...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Advanced Sterilization Products

Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24...

The Issue: Advanced Sterilization Products is recalling certain lots of STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Carefusion 2200 Inc

Recalled Item: 1) Adult Manual Resuscitator Recalled by Carefusion 2200 Inc Due to...

The Issue: CareFusion has received four (4) customer reports of a component (oxygen...

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

Class II — Potential Health HazardOngoing
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Hydroxycobalamin Inj 2500 mcg/ml MDV Recalled by Nora Apothecary and...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Trimix Inj 4.25ml Form MDV Penile Injection Recalled by Nora Apothecary and...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: PHMB Opth Soln 0.02% Recalled by Nora Apothecary and Alternative Therapies,...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Methylcobalamin Inj 1mg/ml MDV Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Folic Acid Inj 5mg/ml MDV Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Renacidin Irrigation: 1000 ml Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund