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. 1,824 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,824 in last 12 months

Showing 2194121960 of 48,330 recalls

DrugMay 10, 2019· Ecolab Inc

Recalled Item: QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol) Recalled by...

The Issue: Incorrect/undeclared excipients: Hand sanitizer was made using the wrong...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 10, 2019· Cadence Science, Inc.

Recalled Item: Cadence Science Pressure Control Glass Syringe Recalled by Cadence Science,...

The Issue: The glass syringe used with Pressure Control Syringes may potentially break...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2019· Teleflex Medical

Recalled Item: Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated...

The Issue: Reported complaints of cracks being observed, prior to use, on swivel wye...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2019· Phadia Ab

Recalled Item: EliA RF IgM Well Recalled by Phadia Ab Due to Potential for reporting low...

The Issue: Potential for reporting low assay results

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: Leadwire sets with snap ends: REF/Catalog Number Description 2106381-001 ECG...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: Replacement leadwires with grabber ends: REF/Catalog Number Description...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: ECG Trunk Cables: REF/Catalog Number Description 2106305-001 ECG Trunk Cable...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: Replacement ECG leadwires with snap ends REF/Catalog Number Description...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: ECG leadwire sets: REF/Catalog Number Description 2106389-001 ECG Leadwire...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

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

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· Cardiocommand Inc.

Recalled Item: CardioCommand Recalled by Cardiocommand Inc. Due to Possible corrosion of...

The Issue: Possible corrosion of the battery contact(s).

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

Class III — Low RiskOngoing
DrugMay 9, 2019· American Health Packaging

Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...

The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2019· American Health Packaging

Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...

The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 9, 2019· I.T.S. GmbH

Recalled Item: Rim Plate Recalled by I.T.S. GmbH Due to The titanium implant has the wrong...

The Issue: The titanium implant has the wrong article number laser marked on it.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2019· Xhale Assurance, Inc.

Recalled Item: Nasal Alar SpO2 Sensor Recalled by Xhale Assurance, Inc. Due to These...

The Issue: These Instructions for Use has missing instructions related to the checking...

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

Class II — Potential Health HazardOngoing
FoodMay 7, 2019· Twin City Foods Inc.

Recalled Item: Signature Kitchens Green Peas & Diced Carrots Recalled by Twin City Foods...

The Issue: Product recalled due to potential for contamination with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugMay 6, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: MethylPREDNISolone Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 6, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.5 mg Recalled by Zydus Pharmaceuticals...

The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 6, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Anastrozole Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to CGMP...

The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 6, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: MethylPREDNISolone Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 6, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: MethylPREDNISolone Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...

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

Class II — Potential Health HazardOngoing
Refund