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

49,150 total recalls
999 in last 12 months

Showing 30341–30360 of 49,150 recalls

Medical DeviceFebruary 24, 2017· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...

The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...

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

Class I — Serious Health HazardOngoing
DrugFebruary 24, 2017· Citron Pharma Llc

Recalled Item: Penicillin V Potassium Tablets Recalled by Citron Pharma Llc Due to Presence...

The Issue: Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 23, 2017· Mckesson Packaging Services

Recalled Item: Aspirin Chewable Tablets Recalled by Mckesson Packaging Services Due to...

The Issue: Presence of Foreign Substance: foreign material found in the bulk inventory.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 23, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Oncology CT - 728243 Computed Tomography X-ray systems...

The Issue: When the user performs a retrospective respiratory gated 4D CT scan with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5 Recalled by Carefusion 2200...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: Thoracentesis/ Paracentesis Kit 10/CS Recalled by Carefusion 2200 Inc Due to...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: ILLINOIS (TJ) NEEDLE ASPIRATION [15GA Recalled by Carefusion 2200 Inc Due to...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP Recalled by Carefusion 2200 Inc Due...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: Manometer Recalled by Carefusion 2200 Inc Due to The integrity of the...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems...

The Issue: Philips identified a 4D CT pulmonary phase issue on Brilliance BigBore...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Enzyme 2 Calibrator Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5 Recalled by Carefusion 2200...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Hill-Rom, Inc.

Recalled Item: TotalCare Bed Systems Recalled by Hill-Rom, Inc. Due to The bed exit alarm...

The Issue: The bed exit alarm may not function properly if the alarm has been armed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Streck

Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...

The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2017· Ace Surgical Supply Co., Inc.

Recalled Item: INFINITY Internal Hex Healing Abutment Recalled by Ace Surgical Supply Co.,...

The Issue: Incorrect device was packaged.

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Labetalol HCl all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Rocuronium Bromide all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Nalbuphine all strengths Recalled by Advanced Pharma Inc. Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Ondansetron HCl all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Fentanyl Citrate and Bupivacaine HCl all strengths Recalled by Advanced...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund