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. 933 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
933 in last 12 months

Showing 44781–44800 of 49,150 recalls

FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 7, 2013· Sagent Pharmaceuticals Inc

Recalled Item: VECURONIUM Bromide for Injection Recalled by Sagent Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: product was not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Novartis Consumer Health

Recalled Item: Parsel Plus ( US product: Excedrin Tension Headache) (Acetaminophen 500...

The Issue: Defective container: products are packaged in pouches which may not have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Novartis Consumer Health

Recalled Item: Excedrin Migraine (Acetaminophen 250 mg Recalled by Novartis Consumer Health...

The Issue: Defective container: products are packaged in pouches which may not have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The product has the potential for solution...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Novartis Consumer Health

Recalled Item: No Doz Recalled by Novartis Consumer Health Due to Defective container:...

The Issue: Defective container: products are packaged in pouches which may not have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Novartis Consumer Health

Recalled Item: Excedrin Extra Strength (Acetaminophen 250 mg Recalled by Novartis Consumer...

The Issue: Defective container: products are packaged in pouches which may not have...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2013· Sybron Dental Specialties

Recalled Item: AOA Mini RPE Screw Assembly Recalled by Sybron Dental Specialties Due to The...

The Issue: The firm initiated the recall of AOA Mini RPE Screw Assembly, because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin (KV)...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BBL Campylobacter CSM Agar (Charcoal-Based Selective Medium) Recalled by...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Endogastric Solutions Inc

Recalled Item: EndoGastric Solutions EsophyX2 Device with Serosa Fastener and Accessories....

The Issue: Endogastric Solutions, Inc. has received a limited number of reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375...

The Issue: Ortho Clinical Diagnostics is recalling CM/RT wear pads which are a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BBL Brucella Laked Blood Agar with Kanamycin and Vancomycin (KV) Recalled by...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL BCYE Selective Agar with PAV Recalled by Becton Dickinson & Co. Due...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL Schaedler K-V Agar with 5% Sheep Blood Recalled by Becton Dickinson &...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL Anaerobe CNA Agar with 5% Sheep Blood // Recalled by Becton Dickinson...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL BBE // CDC Anaerobe Laked Sheep Blood Agar with KV Recalled by Becton...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing