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. 2,634 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,634 in last 12 months

Showing 36813700 of 49,150 recalls

DrugNovember 22, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Javygtor (sapropterin dihydrochloride) Tablets 100mg Recalled by Dr. Reddy's...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· 3M Company - Health Care Business

Recalled Item: Clarity Precision Grip Attachments Recalled by 3M Company - Health Care...

The Issue: Attachments may not mate with the tooth as intended in the digital treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) CATH LAB PACK-LF...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· Medtronic Neuromodulation

Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...

The Issue: Software issues were identified in application version 2.x.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS Recalled...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· Medtronic Neuromodulation

Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...

The Issue: Software issues were identified in application version 2.x.

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

Class II — Potential Health HazardOngoing