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. 1,820 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,820 in last 12 months

Showing 2398124000 of 48,330 recalls

DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Testosterone Enanthate/Cypionate injectable Recalled by Auro Pharmacies,...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Folic Acid injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Methyl-Cobalamin injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Calcium Gluconate injectable Recalled by Auro Pharmacies, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon Natura Model 210-005-152 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon GENILook Model 200-005-152 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon Natura Model 210-105-251 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon GENILook Model 200-005-153 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon GENILook Model 200-105-151 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon GENILook Model 200-005-151 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon Natura Model 210-005-051 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon Natura Model 210-005-251 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon Natura Model 210-005-151 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon GENILook Model 200-005-251 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon GENILook Model 200-105-252 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon GENILook Model 200-105-251 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon GENILook Model 200-105-152 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Genicon, Inc.

Recalled Item: Genicon Natura Model 210-005-052 Recalled by Genicon, Inc. Due to There is...

The Issue: There is potential for the plastic optical tip to become detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: These catheters may have the following deficiencies: 1) barium sulfate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: These catheters may have the following deficiencies: 1) barium sulfate...

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

Class II — Potential Health HazardOngoing