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 2016120180 of 28,579 recalls

Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA GDE upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due to...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard ventilator- Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard with Compressor ventilator- Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: TCA Board Recalled by Carefusion 211 Inc dba Carefusion Due to CareFusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: Gas Delivery Engine (GDE)- Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: Gas Delivery Engine (GDE) Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA GDE/UIM upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: Gas Delivery Engine (GDE)-1st Generation Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Zimmer Gmbh

Recalled Item: Dome Centric component ( 01.04227.005) from the Anatomical Shoulder (AS)...

The Issue: In some cases it has been difficult or not possible to disassemble the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· CSL Behring GmbH

Recalled Item: Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS) Recalled by CSL...

The Issue: Reagent lots # 15243MA and 15243MB shows a reduced stability once opened...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard with Compressor ventilator Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Comprehensive ventilator- Recalled by Carefusion 211 Inc dba Carefusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics...

The Issue: If the user selects the Comment or Interpretation option (in the enGEN .gsb...

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

Class III — Low RiskOngoing
Medical DeviceMay 16, 2016· FSC Laboratories, Inc

Recalled Item: Flexichamber Anti-Static Valved Collapsible Holding Chamber Recalled by FSC...

The Issue: Product had torn/loose seal around the mouthpiece.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2016· Lifeline First Aid LLC

Recalled Item: Item # 4042-CPR Rescue Kit Recalled by Lifeline First Aid LLC Due to First...

The Issue: First aid kits or rescue kits are recalled because they contains the CPR...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2016· Lifeline First Aid LLC

Recalled Item: 5195GM Recalled by Lifeline First Aid LLC Due to Cadillac First Aid Kit is...

The Issue: Cadillac First Aid Kit is recalled because it contains the CPR Shield with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2016· Medtronic Sofamor Danek Usa, Inc - Dallas Distribution

Recalled Item: Saw Sagittal Catalog Number: ES 300 Recalled by Medtronic Sofamor Danek Usa,...

The Issue: Medtronic Powered Surgical Solutions testing of the Sagittal Saw Rocker Arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing