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 2810128120 of 28,579 recalls

Medical DeviceApril 30, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Rejuvenate Modular Stems Stryker Ireland Carrigtwohill Industrial Estate...

The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2012· Zimmer Inc.

Recalled Item: Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral Recalled...

The Issue: The design of the spring clip for the jaw assembly was updated in March 2011...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2012· Accutron Inc

Recalled Item: CM Flowmeter Pkg H Recalled by Accutron Inc Due to Accutron is recalling the...

The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2012· Accutron Inc

Recalled Item: Newport Portable Package Recalled by Accutron Inc Due to Accutron is...

The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2012· Accutron Inc

Recalled Item: Ultra PC% Cabinet Mount Package G Recalled by Accutron Inc Due to Accutron...

The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2012· Accutron Inc

Recalled Item: Flow Meter Recalled by Accutron Inc Due to Accutron is recalling the...

The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2012· Plasma Surgical Inc.

Recalled Item: PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma...

The Issue: Potential failure in the glued seal between the stem and the tip of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2012· Motorola Inc

Recalled Item: Motorola Solutions PCS3000/CS3070 Laser Utility/Peripheral Laser Products...

The Issue: It was discovered the CS3000/CS3070 was manufactured using the laser power...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2012· Kimberly-Clark Corporation

Recalled Item: Kimberly Clark Patient Warming System - Model 1000 Control Unit. Recalled by...

The Issue: A defect of the "fuse holder" can lead to a Control Unit failure that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2012· MicroAire Surgical Instruments, LLC

Recalled Item: Lipofilter 3000 Recalled by MicroAire Surgical Instruments, LLC Due to...

The Issue: Medical device was not manufactured under Good Manufacturing Procedures and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2012· Ormco/Sybronendo

Recalled Item: The brand name of the device is Damon 3MX Bicuspid Bracket Recalled by...

The Issue: The firm initiated the recall as a result of a misidentification of the...

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

Class III — Low RiskOngoing
Medical DeviceApril 23, 2012· Sigma

Recalled Item: SIGMASpectrum Infusion Pump Master Drug Library (MDL) Editor software....

The Issue: Sigma is a safety alert for the Master Drug Library (MDL) Editor software...

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

Class III — Low RiskOngoing
Medical DeviceApril 23, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential issue due to image...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2012· Roche Molecular Systems, Inc.

Recalled Item: Amplilink (AL) Software 3.2.3 for use with COBAS AMPLICOR Recalled by Roche...

The Issue: When using a Laboratory Information system (LIS) with automated systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Putty Multiple Sizes Grafton is a human bone Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Matrix Strips Multiple Sizes Grafton is a human Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Matrix PLF Multiple Sizes Grafton is a human Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Optimum Expanse S Multiple sizes Grafton is a human bone Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing