Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,678 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,678 in last 12 months

Showing 33813400 of 13,379 recalls

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
DrugJanuary 26, 2022· AuroMedics Pharma LLC

Recalled Item: Polymyxin B for Injection USP Recalled by AuroMedics Pharma LLC Due to...

The Issue: Presence of Particulate Matter; product complaint of hair discovered in a...

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

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: 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: ELECTROLYTE Supplement Tablets (calcium 5.2 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: Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamabrom 25mg) Recalled...

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: CETAFEN COUGH & COLD COUGH & 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: REMfresh Advanced Ion-Powered Melatonin (Melatonin 5 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: SINUS DECONGESTANT Nasal Decongestant (phenylephrine HCl 5mg) 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: Cold Tablet Pain Reliever/Fever Reducer/Expectorant/Nasal Decongestant...

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: Regular Strength Pain Reliever (acetaminophen 110 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: AYPANAL Non-aspirin Pain Reliever (acetaminophen 325 mg) tablets 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: Cold Relief Severe Pain/Cough (acetaminophen 325mg 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: SINU-PHEN PLUS sinus pain and congestion tabs (acetaminophen 500 mg Recalled...

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: Exaprin pain reliever (acetaminophen 110 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: EXTRA STRENGTH UN-ASPIRIN (acetaminophen 500 mg) 2 Caplet packets Recalled...

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 250mg) 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: Extra Strength (ES) PAIN RELIEVER (acetaminophen 500 mg) 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: Sinus Relief (acetaminophen 325mg 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