Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,484 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,484 in last 12 months

Showing 1360113620 of 27,558 recalls

Medical DeviceMay 1, 2019· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and...

The Issue: The 0-arm 1000 Imaging System uses energy from the batteries to generate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2019· Abbott Vascular

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

The Issue: Reports of implantable mitral valve repair system clips unexpectedly opening...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Item code: 8881200029 Recalled by...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject" 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing