Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,535 in last 12 months

Showing 86018620 of 48,219 recalls

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
FoodMay 17, 2023· HU PRODUCTS

Recalled Item: Hu Vanilla Crunch Dark Chocolate bar Recalled by HU PRODUCTS Due to...

The Issue: may contain undeclared tree-nuts

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
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