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

48,330 total recalls
960 in last 12 months

Showing 33821–33840 of 48,330 recalls

DrugFebruary 5, 2016· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...

The Issue: PRESENCE OF PARTICULATE MATTER: Product complaint for the presence of...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2016· Teva Pharmaceuticals USA

Recalled Item: Paricalcitol Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2016· AstraZeneca Pharmaceuticals LP

Recalled Item: Tudorza Pressair (aclindinium bromide inhalation powder) Recalled by...

The Issue: Defective Delivery System: Some units have actuation counters set to a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano SpinVision Sterile Equip cover II Recalled by Volcano Corporation...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano R100 Sterile Equipment Cover Recalled by Volcano Corporation Due to...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Beckman Coulter Inc.

Recalled Item: Allegra X-5 rotor yoke Recalled by Beckman Coulter Inc. Due to A defective...

The Issue: A defective rotor yoke on Allegra X-5 allows improper rotor seating on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64:Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray Systems Recalled by Philips...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Computed Tomography X-ray Systems Recalled by Philips...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostic ADVIA Centaur Calibrator E- 6- Pack ()...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E- 6- Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Abbott Vascular

Recalled Item: MitraClip Clip Delivery System Recalled by Abbott Vascular Due to Abbott...

The Issue: Abbott Vascular has recently received reports of cases on Clip Delivery...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Draeger Medical, Inc.

Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...

The Issue: The battery capacity of the optional PS500 power supply unit for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Perfusion Tubing Pack Recalled by Medtronic Perfusion...

The Issue: Medtronic is notifying customers who have or may receive specific lots of...

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

Class III — Low RiskOngoing