Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 930 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
930 in last 12 months

Showing 47721–47740 of 49,150 recalls

FoodJuly 17, 2012· Gills Onions, LLC

Recalled Item: Diced Red Tomatoes Recalled by Gills Onions, LLC Due to Potential Listeria...

The Issue: Gills Onions is recalling diced and slivered red and yellow onions and diced...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 17, 2012· Gills Onions, LLC

Recalled Item: Slivered Yellow Sweet Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered red and yellow onions and diced...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
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· 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· 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: DataInnovations (Instrument Manager) (version 8.04) interfaces middleware...

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 LC (version 3.0) is a sample preparation 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· Roche Molecular Systems, Inc.

Recalled Item: DataCare POC  is an information management system that provides 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· Stryker Howmedica Osteonics Corp.

Recalled Item: Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral...

The Issue: Stryker has become aware that insufficient taper torsional strength may...

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 COBAS 8000 data manager modular analyzer series (all versions) 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: 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· Roche Molecular Systems, Inc.

Recalled Item: LightCycler 2.0 Instrument (software version 4.1) is a Rapid PCR 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· 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
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