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. 2,469 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,469 in last 12 months

Showing 2494124960 of 27,373 recalls

Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CK Slides packaged as 300 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CRBM Slides packaged as 90 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products TRIG Slides packaged as 300 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products BUN/UREA Slides packaged as 300 slides/pack...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products dHDL Slides packaged as 300 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHBR Slides packaged as 90 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products AST Slides packaged as 300 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products LAC Slides packaged as 300 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Accelerated Care Plus Corporation

Recalled Item: Omnicycle Elite Recalled by Accelerated Care Plus Corporation Due to An...

The Issue: An anomaly in the firmware that may cause Omnicycle Elite to operate at a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Physio Control, Inc.

Recalled Item: The LIFEPAK 500 Automated External Defibrillator is a semi-automatic...

The Issue: The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes CMF Distraction System The product is intended for use Recalled by...

The Issue: The firm initiated a voluntary recall of the BC Distractor Body which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Inegra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing