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. 2,491 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,491 in last 12 months

Showing 1880118820 of 28,140 recalls

Medical DeviceDecember 13, 2016· US Endoscopy Group Inc

Recalled Item: Roth Net Polyp Retrieval Recalled by US Endoscopy Group Inc Due to The firm...

The Issue: The firm was notified that the expiration date on the outer carton is...

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

Class III — Low RiskOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Bio mCT-S(40) 3R->4R Upgrade Recalled by Siemens Medical Solutions USA Inc....

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· On-X Life Technologies, Inc.

Recalled Item: Chord-X Chordal Sizer is designed to assist in determining the Recalled by...

The Issue: Four issues were uncovered by the recalling firm's CAPA: 1) Burrs were found...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(40)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(64)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(40)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(64)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT X-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Pentax of America Inc

Recalled Item: Rigid Laryngostroboscopes The Rigid Laryngostroboscopes Recalled by Pentax...

The Issue: Pentax is initiating a Field Correction to revise the Instructions for Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The...

The Issue: Olympus has received complaints regarding the breakage of the endoscope's...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope Recalled...

The Issue: Olympus is recalling the URF-P6/P6R endoscopes due to a similar device...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Medtronic Navigation, Inc.

Recalled Item: AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the AxIEM...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Great Basin Scientific, Inc.

Recalled Item: Great Basin Staph lD/R Blood Culture Panel The Great Basin Recalled by Great...

The Issue: The Great Basin Staph ID/R Panel is being recalled because the S. aureus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· MEDLINE IND

Recalled Item: Medline E-Z Lubricating Jelly Recalled by MEDLINE IND Due to Product was not...

The Issue: Product was not sterilized. Product was shipped to distribution centers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Bard Access Systems

Recalled Item: StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Recalled...

The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System Recalled...

The Issue: Merge received reports of Merge Eye Station being unable to capture images...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Bard Access Systems

Recalled Item: StatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged...

The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q/Q.zen Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens initiated a corrective action to address two possible, mutually...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products UPRO Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: There is a potential for variable negatively and positively biased urine...

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

Class II — Potential Health HazardOngoing