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. 2,453 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,453 in last 12 months

Showing 2616126180 of 28,579 recalls

Medical DeviceJune 10, 2013· Radiometer America Inc

Recalled Item: pO2 D999 membrane units. Distributed by Radiometer America Recalled by...

The Issue: RADIOMETER became aware that the regarded lot pO2 units 942-042R0971 were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Staar Surgical Co.

Recalled Item: Afinity CQ2015A Intraocular Lens The visual correction of aphakia in...

The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Getinge Assure Accufast BI Test Pack w/ 25 Controls Recalled by Steritec...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Medline Med-Checks BI Test packs with Instant Readout Integrator Recalled by...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Mesa Labs Smart-Read 10^5 EZ Test BI Test Pack Recalled by Steritec Products...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Biomet 3i, LLC

Recalled Item: Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product...

The Issue: One of the dental implants do not have the internal hex feature. One of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Dynamics Information System (sDIS) versions 9.5 and VA10A. The...

The Issue: Siemens initiate this recall due to a potential issue when using the sDIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Getinge Assure Accufast BI Test Pack w/ 5 Controls Recalled by Steritec...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System PS Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System CPS Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System CR Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Cardinal Steam Biological Indicator Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Staar Surgical Co.

Recalled Item: nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years...

The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Medline Steam Biological Indicators Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Dual Camera Controller Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Instrument Control Box Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Surgeon Side Cart Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing