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. 1,743 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,743 in last 12 months

Showing 4234142360 of 49,150 recalls

Medical DeviceFebruary 7, 2014· Draeger Medical Systems, Inc.

Recalled Item: Draeger PS500 Power Supply Unit of the Infinity ACS Workstation Recalled by...

The Issue: The battery capacity of the optional PS500 Power Supply Unit of the Infinity...

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

Class I — Serious Health HazardOngoing
DrugFebruary 7, 2014· Actavis

Recalled Item: Gelnique (oxybutynin chloride) Gel 10% Recalled by Actavis Due to Subpotent...

The Issue: Subpotent Drug: Drug potency was compromised during shipment.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 7, 2014· Natural Grocers by Vitamin Cottage

Recalled Item: Natural Grocers brand Dark Chocolate Almonds Recalled by Natural Grocers by...

The Issue: Natural Grocers by Vitamin Cottage is recalling one lot of six ounce...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2014· Medtronic Vascular

Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...

The Issue: Incorrect master label.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 6, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...

The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Synthes, Inc.

Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...

The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Fisher Scientific Co

Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...

The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Alere San Diego, Inc.

Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...

The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F200NRe High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...

The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F160NRe High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing