Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,067 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,067 in last 12 months

Showing 14001–14020 of 29,201 recalls

Medical DeviceMay 1, 2019· Abbott Laboratories, Inc

Recalled Item: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Recalled by...

The Issue: Mixer blade may separate from mixer due to the screw and nut failure and...

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· 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
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· Stryker GmbH

Recalled Item: Endotrac ECTR 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
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 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