Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,495 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,495 in last 12 months

Showing 2058120600 of 49,677 recalls

Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 Recalled by...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 3 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosie4 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
FoodSeptember 30, 2019· Jumbo Foods, Inc.

Recalled Item: Wedge Chicken Salad Recalled by Jumbo Foods, Inc. Due to Potential Listeria...

The Issue: Product is recalled due to a potential for contamination with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 30, 2019· Jumbo Foods, Inc.

Recalled Item: Chipotle Chicken Salad Recalled by Jumbo Foods, Inc. Due to Potential...

The Issue: Product is recalled due to a potential for contamination with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 30, 2019· Jumbo Foods, Inc.

Recalled Item: Bacon Ranch Chicken Salad Recalled by Jumbo Foods, Inc. Due to Potential...

The Issue: Product is recalled due to a potential for contamination with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 30, 2019· Jumbo Foods, Inc.

Recalled Item: Cranberry Chicken Salad Recalled by Jumbo Foods, Inc. Due to Potential...

The Issue: Product is recalled due to a potential for contamination with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 30, 2019· Jumbo Foods, Inc.

Recalled Item: Chicken Salad Recalled by Jumbo Foods, Inc. Due to Potential Listeria...

The Issue: Product is recalled due to a potential for contamination with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing