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. 2,479 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,479 in last 12 months

Showing 2110121120 of 49,150 recalls

DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Club Pack Display Recalled by Medtech Products,...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Redness Relief Club Pack Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Assorted Sidekick Floor Stand Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Redness and Itchy Eye Relief Sidekick Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Hand Pocket Pal Tray Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 26, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Surgical System Recalled by Intuitive Surgical,...

The Issue: The firm become aware of a potentially defective capacitors on circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci X Surgical System Surgical System Recalled by Intuitive Surgical,...

The Issue: The firm become aware of a potentially defective capacitors on circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Surgical System Recalled by Intuitive Surgical, Inc. Due to The...

The Issue: The firm become aware of a potentially defective capacitors on circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2019· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed Carestation CS1 - Product Usage: The device can Recalled by...

The Issue: Fasteners potentially torqued to a value less than the specified value and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Push Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: WS80A Diagnostic Ultrasound System Version 1.00.16 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: HS70A Diagnostic Ultrasound System Version 2.01.00 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing