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 2358123600 of 27,373 recalls

Medical DeviceApril 14, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...

The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Ready Pack Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Potential for biased...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD 100 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Bicarbonate Concentrate Recalled by Fresenius Medical Care...

The Issue: Naturalyte Liquid Bicarbonate maybe contaminated

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD 500 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Recalled by Siemens Healthcare Diagnostics,...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD Total 100 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Synthes, Inc.

Recalled Item: Synthes External Fixation Systems (Small Recalled by Synthes, Inc. Due to...

The Issue: Labeling changes have been made related to MR (Magnetic Resonance imaging)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation Systems (enGen) with TCAutomation -- For in...

The Issue: Software anomaly: potential for delay in the reporting of patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems BRAHMS PCT 100 test Sold only OUS Recalled by Siemens...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae Recalled by...

The Issue: Potential for separation of dilator tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Cochlear Americas Inc.

Recalled Item: Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to Recalled by...

The Issue: Cochlear America is recalling Cochlear Baha Soft Tissue Gauge due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo...

The Issue: Potential for separation of dilator tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When the E-NMT-01 module...

The Issue: When the E-NMT-01 module is used in conjunction with the ElectroSensor, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Philips Medical Systems, Inc.

Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...

The Issue: In special cases, during the start-up of the current model of MobileDiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam -emission computed tomography system Used to detect or image Recalled...

The Issue: There is a potential for patient finger injury on the e.cam systems.

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

Class II — Potential Health HazardOngoing