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. 2,678 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,678 in last 12 months

Showing 63016320 of 29,298 recalls

Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX -i Neonatal Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Small Adult Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Pediatric Recalled by Maquet Medical Systems USA Due to 1. An...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: BEQ-HMO 50000-USA/ QUADROX-i Small Recalled by Maquet Medical Systems USA...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX -i Neonatal Recalled by Maquet Medical Systems USA Due to 1. An...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iD Pediatric Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: BEQ-HMOD70000-USA/QUADROX-iD Recalled by Maquet Medical Systems USA Due to...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to 1. An accessory may...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to 1. An...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Pediatric Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Small Adult Recalled by Maquet Medical Systems USA Due to 1. An...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to Product packaging...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: BEQ-HMO 71000-USA /QUADROX-i Adult Recalled by Maquet Medical Systems USA...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: HMOD 70000-USA/QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Bryan Medical Inc

Recalled Item: Aeris Balloon Dilation Catheter Recalled by Bryan Medical Inc Due to Mislabeling

The Issue: Devices were mislabeled.

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

Class II — Potential Health HazardOngoing