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. 1,069 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,069 in last 12 months

Showing 9901–9920 of 27,373 recalls

Medical DeviceMarch 10, 2021· Remel Inc

Recalled Item: Remel Haemophilus Test Medium(100mm) 10/PK Recalled by Remel Inc Due to When...

The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2021· Remel Inc

Recalled Item: Remel Haemophilus Test Medium (150 mm) 10/PK Recalled by Remel Inc Due to...

The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2021· Medtronic Neuromodulation

Recalled Item: A610 Clinician Programmer Application for Deep Brain Stimulation Clinician...

The Issue: There are two issues within this correction action: 1. Cycling Issue: When...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Ilestro 7 VR-T Recalled by BIOTRONIK Inc Due to There is a...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Ilestro 7 VR-T DX Recalled by BIOTRONIK Inc Due to There is a...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· Arrow International Inc

Recalled Item: Arrow OnControl Bone Lesion Biopsy System Tray-11 ga 10 cm Recalled by Arrow...

The Issue: Difficulty inserting the biopsy ejector rod into the bone lesion biopsy...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK IPERIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA NEO 7 VR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Ilestro 7 DR-T Recalled by BIOTRONIK Inc Due to There is a...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK IPERIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iperia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing