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. 2,439 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,439 in last 12 months

Showing 2902129040 of 49,150 recalls

FoodMay 11, 2017· Trident Seafoods Corp - Island Enterprise M/V

Recalled Item: Trident Item # 16596 Recalled by Trident Seafoods Corp - Island Enterprise...

The Issue: Alaska Cod Diamond Cut Squares 3 oz product is recalled because they may...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2017· Lamb Weston Inc

Recalled Item: Red Robin Burgers and Brews Crispy Onion Rings Recalled by Lamb Weston Inc...

The Issue: Red Robin Burgers and Brews Crispy Onion Rings, 14 oz. retail packages, are...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 11, 2017· Trident Seafoods Corp - Island Enterprise M/V

Recalled Item: Trident Item # 16582 Recalled by Trident Seafoods Corp - Island Enterprise...

The Issue: Alaska Cod Rectangles 4 oz product is recalled because they may contain...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2017· Trident Seafoods Corp - Island Enterprise M/V

Recalled Item: Trident Item # 16595 Recalled by Trident Seafoods Corp - Island Enterprise...

The Issue: Alaska Cod Squares 4 oz product is recalled because they may contain small...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2017· Trident Seafoods Corp - Island Enterprise M/V

Recalled Item: Trident Item # 38520 Recalled by Trident Seafoods Corp - Island Enterprise...

The Issue: Panko Breaded Alaska Cod 4 oz. product is recalled because it may contain...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2017· Trident Seafoods Corp - Island Enterprise M/V

Recalled Item: Trident Item # 474568 Recalled by Trident Seafoods Corp - Island Enterprise...

The Issue: Irregulars Breaded Cod 2 oz. 10 Grain Cod product is recalled because it may...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system Recalled by...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Philips Electronics North America Corporation

Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...

The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Teleflex Medical

Recalled Item: Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets...

The Issue: Product size listed on the labeling is incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Brivo MR355 Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Signa PET/MR (K163619 Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Discovery MR750 3.0T Product Usage: Intended use: The Discovery MR750...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: SIGNA Creator Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Argon Medical Devices, Inc

Recalled Item: Clear Flashback Needle 7cm x 18G AMC/4 Recalled by Argon Medical Devices,...

The Issue: Argon Medical has received a complaint from one of their distributors of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDxt Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· Medtronic Navigation, Inc.

Recalled Item: Install CD Recalled by Medtronic Navigation, Inc. Due to Software issue...

The Issue: Software issue related to the StealthStation S7 system and the Synergy Spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· Zimmer Biomet Spine Inc.

Recalled Item: Vitality Spinal Fixation System Recalled by Zimmer Biomet Spine Inc. Due to...

The Issue: Zimmer Biomet is conducting a medical device recall for Vitality T27 Final...

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

Class II — Potential Health HazardOngoing