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. 2,466 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,466 in last 12 months

Showing 2500125020 of 28,579 recalls

Medical DeviceJanuary 6, 2014· Boston Scientific Corporation

Recalled Item: Atlantis PV Recalled by Boston Scientific Corporation Due to Reports of...

The Issue: Reports of physicians experiencing inability to pass a 0.035" guidewire...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 3, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix L/P with Echo PS 10" X 13" Product Code Recalled by Davol, Inc.,...

The Issue: Product labeling does not match product configuration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix L/P with Echo PS 6" X 8" Product Code Recalled by Davol, Inc.,...

The Issue: Product labeling does not match product configuration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 1, 2014· Abbott Point Of Care Inc.

Recalled Item: i-STAT G3+ Cartridge pH Recalled by Abbott Point Of Care Inc. Due to Abbott...

The Issue: Abbott Point of Care has determined that some individual patient results...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 2 Rover Ultra Waste Management System Recalled by Stryker...

The Issue: The purpose of this correction is to upgrade the Neptune 2 Waste Management...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 2 Rover Ultra Waste Management System. Recalled by Stryker...

The Issue: The purpose of this correction is to upgrade the Neptune 2 Waste Management...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. The...

The Issue: GE Healthcare has recently become aware of potential safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: The Gaymar Medi-Therm device provides a means of regulating patient Recalled...

The Issue: Stryker Medical has identified that on some units of the MTA7900, there is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2013· Carestream Health, Inc.

Recalled Item: KODAK DirectView DR 7500 Dual Detector System Recalled by Carestream Health,...

The Issue: Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2013· Vital Signs Colorado Inc.

Recalled Item: Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for...

The Issue: A circuit in use was occluded by a blue port cap that was inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 87" (221 cm) Appx 2.9 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 5" Smallbore Ext Set w/MicroClave¿ T-Connector Recalled by ICU Medical, Inc....

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.31 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 5" Smallbore Ext Set w/MicroClave¿ T-Connector Recalled by ICU Medical, Inc....

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 78" Ext Set w/2 BCV-Clave¿ Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.58 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 103" (262 cm) Appx 3.9 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 14" (36 cm ) Appx 0.50 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 28" (71 cm) Appx 1.0 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing