Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,937 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,937 in last 12 months

Showing 2300123020 of 52,570 recalls

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
DrugApril 30, 2019· Sagent Pharmaceuticals Inc

Recalled Item: Ketorolac Tromethamine Injection Recalled by Sagent Pharmaceuticals Inc Due...

The Issue: Lack of Sterility Assurance: Microbial growth detected during a routine...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2019· Par Pharmaceutical, Inc.

Recalled Item: Mycophenolate Mofetil for Injection Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Presence of Particulate Matter; glass fragment observed in one vial of...

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

Class I — Serious Health HazardOngoing
Refund
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