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. 2,608 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,608 in last 12 months

Showing 1012110140 of 49,150 recalls

Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit- For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
DrugJanuary 6, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Rocuronium Bromide Injection Recalled by Nephron Sterile Compounding Center...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· MACLEODS PHARMA USA, INC

Recalled Item: Levofloxacin Tablets Recalled by MACLEODS PHARMA USA, INC Due to Mismatching...

The Issue: Mismatching of the embossing on the tablets (T7) with the embossing...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 5, 2023· S & MOHR AMERICA, S.A. DE C.V.

Recalled Item: abm Respiratory Care Standart Breating Circuit with Face Mask - Recalled by...

The Issue: Incorrect expiration date on product label. The manufacturing date was...

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

Class III — Low RiskOngoing
DrugJanuary 4, 2023· Intersect ENT, Inc.

Recalled Item: SINUVA (mometasone furoate) sinus implant Recalled by Intersect ENT, Inc....

The Issue: Failed Dissolution Specification; product did not meet the average 24-hour...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 4, 2023· Wishbone Medical, Inc.

Recalled Item: WishBone Medical Smart Correction Dual Joint Express Struts Recalled by...

The Issue: Firm identified that user may be unable to adjust the length of the Smart...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2023· Bard Peripheral Vascular Inc

Recalled Item: Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter...

The Issue: Due to the adhesive provided within the catheter repair kits maybe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2023· Western/Scott Fetzer Company

Recalled Item: Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR Recalled by...

The Issue: Gauge malfunction: Digital gauge displays an incorrect tank pressure -...

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

Class II — Potential Health HazardOngoing
DrugDecember 30, 2022· Northern VA Compounders PLLC

Recalled Item: QuadMix Plus (PGE1/Papaverine HCl/Phentolamine Mesylate/Atropine)...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2022· Northern VA Compounders PLLC

Recalled Item: TriMix Injection (PGE1/Papaverine HCl/Phentolamine Mesylate)...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2022· Northern VA Compounders PLLC

Recalled Item: TriMix Injection (PGE1/Papaverine HCl/Phentolamine Mesylate)...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2022· Northern VA Compounders PLLC

Recalled Item: Methylcobalamin Injection Solution Recalled by Northern VA Compounders PLLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2022· Northern VA Compounders PLLC

Recalled Item: QuadMix Injectable (PGE1/Papaverine HCl/Phentolamine Mesylate/Atropine)...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2022· Northern VA Compounders PLLC

Recalled Item: BiMix STD 001 (Papaverine HCl/Phentolamine Mesylate) 30mg/1mg/mL INJECTABLE...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund