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. 1,069 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,069 in last 12 months

Showing 13321–13340 of 49,150 recalls

DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: ARMOUR THYROID (thyroid tablets Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: RIVASTIGMINE TRANSDERMAL SYSTEM Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Enoxaparin Sodium Injection Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 26, 2022· Siren Snacks

Recalled Item: Siren Birthday Cake Protein Bites Recalled by Siren Snacks Due to Undeclared...

The Issue: Undeclared cashews and almond butter allergens

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2022· Blaine Labs Inc

Recalled Item: REVITADERM WOUND CARE GEL Recalled by Blaine Labs Inc Due to Microbial...

The Issue: Microbial Contamination of Non-sterile Product; FDA analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: MIRALAC (calcium carbonate 420mg) tablets Recalled by Ultra Seal Corporation...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: AERO TAB Cold Relief (acetaminophen 325 mg Recalled by Ultra Seal...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Nasal & Sinus Decongestant (phenylephrine HCl 5mg) 2 tablets per packet...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: REMfresh Advanced Ion-Powered Melatonin (Melatonin 2 mg) Caplets Recalled by...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: FEM-PRIN MENSTRUAL RELIEF (acetaminophen 325 mg Recalled by Ultra Seal...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: MAGNACAL (calcium carbonate 420 mg) Recalled by Ultra Seal Corporation Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: DBI 357 Super Magnum Quick Energy Stimulant (caffeine 200mg) tablets...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: MidNite Sleep Health (melatonin 1.5 mg) tablets Recalled by Ultra Seal...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg Recalled by...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: PEPTIME Energy (caffeine 300mg) tablets Recalled by Ultra Seal Corporation...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Cold Relief (acetaminophen 250 mg Recalled by Ultra Seal Corporation Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: PAINAID (acetaminophen 110 mg Recalled by Ultra Seal Corporation Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: PAINAID BRF Back Relief Formula (acetaminophen 250 mg Recalled by Ultra Seal...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: CONGESTAID II Nasal Decongestant (Phenylephrine HCl 5mg) 2 tablet packets...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Lite Remfresh Advanced Ion-Powered Melatonin (Melatonin 0.5mg) Tablets...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund