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 2770127720 of 28,579 recalls

Medical DeviceJuly 19, 2012· Abbott Point Of Care Inc.

Recalled Item: Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 Recalled by...

The Issue: Abbott Point of Care (APOC) has determined that for the Cliniqa Liquid QC...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder Liner 40mm Recalled by Zimmer, Inc. Due to...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-029-00- Trabecular Metal Reverse Shoulder Liner 36mm Recalled by...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Shiley Reusable Cannula Low Pressure Cuffed Tracheostomy Tubes Recalled by...

The Issue: Covidien is recalling certain cuffed Shiley tracheostomy tubes due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-028-01 - Trabecular Metal Reverse Shoulder Liner 40mm 65¿ Neck...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-029-01 - Trabecular Metal Reverse Shoulder Liner 36 mm 65¿¿ Recalled...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Imaging XS. Radiological image processing system. Recalled by Siemens...

The Issue: There is a potential malfunction when using syngo Imaging XS, version VA70A...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to There is a...

The Issue: There is a potential malfunction in which a miscalculation occurs for images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...

The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...

The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) Vancomycin Flex(R) Reagent Cartridge (VANC Recalled by...

The Issue: Siemens has received complaints of customers experiencing slopes >1.05 when...

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

Class III — Low RiskOngoing
Medical DeviceJuly 17, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) Reagent Management System (RMS) - Power Cord. The Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed that partial insertion of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Conformis Inc

Recalled Item: Conformis iTotal CR-Cruciate Retaining Knee Replacement System Model...

The Issue: Addendum Labeling iTotal CR Surgical Technique with Detailed Instructions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay Recalled by Siemens Healthcare...

The Issue: Syphilis Assay Interference with HBsAg Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2012· Roche Molecular Systems, Inc.

Recalled Item: DataCara GM is an information management system that provides data Recalled...

The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2012· Encore Medical, Lp

Recalled Item: djo surgical Screw 6.5 mm Recalled by Encore Medical, Lp Due to Mislabeling

The Issue: One lot of the 010-55-030, 6.5 mm Cancellous Bone Screw was recalled because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2012· Roche Molecular Systems, Inc.

Recalled Item: LightCycler 1.2 (software version 3.5) is a Rapid PCR analyzer Recalled by...

The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2012· Roche Molecular Systems, Inc.

Recalled Item: Data Station AMPLILINK software is an instrument user interface/ data...

The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2012· Roche Molecular Systems, Inc.

Recalled Item: The MagNA Pure 96 System (versions 1.0 and 2.0) is Recalled by Roche...

The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2012· Animas Corporation

Recalled Item: IR1200 Recalled by Animas Corporation Due to Wear of the keypad that may...

The Issue: Wear of the keypad that may lead to damage such as tearing or peeling of the...

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

Class II — Potential Health HazardOngoing