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. 2,507 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,507 in last 12 months

Showing 1864118660 of 49,677 recalls

Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Premium Urine Meter Foley Tray Recalled by Covidien Llc...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400mL Recalled by Covidien Llc Due to Temperature sensing catheters...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Foley Catheter with Temperature 16FR 5CC2W Recalled by...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Foley Catheter with Temperature Sensor 14FR 5CC2W...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Premium Urine Meter Tray 400mL Recalled by Covidien Llc...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
FoodApril 27, 2020· Condies Foods, Inc.

Recalled Item: 43237 ROLL chicken salad on croissant single Recalled by Condies Foods, Inc....

The Issue: Undeclared SOY allergen. Wrong ingredient purchased and used.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 27, 2020· Condies Foods, Inc.

Recalled Item: 43559 SNDW Chicken Sandwich on White Single Recalled by Condies Foods, Inc....

The Issue: Undeclared SOY allergen. Wrong ingredient purchased and used.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Philips North America, LLC

Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...

The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2020· Dr. Reddy's Laboratories, Inc.

Recalled Item: Esomeprazole Magnesium Delayed Release Capsules USP Recalled by Dr. Reddy's...

The Issue: Discoloration: product contains brown pellets

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY 1/2 CONN W/LL STRLE 24 REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Vein Irrigation Cannula with blunt tip. ASY VIC Recalled by LivaNova USA...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing