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. 2,630 recalls have been distributed to Nebraska in the last 12 months.
Showing 4981–5000 of 13,356 recalls
Recalled Item: Aurobindo Ranitidine Caspules 150 mg Recalled by AuroMedics Pharma LLC Due...
The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DG Health Acid Reducer Ranitidine Tablets 150 mg Recalled by AuroMedics...
The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP) Recalled by American Health...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5...
The Issue: Presence of Foreign Substance: Black particles were found in the lots during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LETS GEL KIT Convenience Pack (To prepare 100 mL LETS GEL) Recalled by...
The Issue: Microbial contamination of non-sterile product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate Recalled by Avantor Performance Materials Inc Due to...
The Issue: Failed Stability Specifications: Product exceeds compendia and firm's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lannett Ranitidine Syrup (Ranitidine Oral Solution Recalled by Lannett...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 500 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE INJECTION Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 100 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.