Product Recalls in Ohio

Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,790 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,790 in last 12 months

Showing 35413560 of 13,469 recalls

DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Ceftazidime Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

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 6, 2021· Edge Pharma, LLC

Recalled Item: Vancomycin HCl in 0.9 % Sodium Chloride Injection Recalled by Edge Pharma,...

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 6, 2021· Edge Pharma, LLC

Recalled Item: Lidocaine HCl/Phenylephrine HCl Nasal Solution Recalled by Edge Pharma, LLC...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: LT Topical Cream Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Trypan Blue 0.03% Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 Recalled by Dental...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree sample boxes Recalled by Dental Alliance Holdings LLC Due to...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx7 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx26 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Gilead Sciences, Inc.

Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: investigation into a customer complaint...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx21 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx36 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Akorn, Inc.

Recalled Item: Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles...

The Issue: Labeling: Missing Label

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Akorn, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Akorn, Inc. Due to...

The Issue: Labeling: Missing Label

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

Class III — Low RiskOngoing
Refund
DrugDecember 2, 2021· Torrent Pharma Inc.

Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 1, 2021· Torrent Pharma Inc.

Recalled Item: Telmisartan and Hydrochlorothiazide Tablets Recalled by Torrent Pharma Inc....

The Issue: Superpotent; Hydrochlorothiazide

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

Class III — Low RiskOngoing
Refund
DrugNovember 30, 2021· Pfizer Inc.

Recalled Item: 5% Dextrose Injection Recalled by Pfizer Inc. Due to Lack of sterility...

The Issue: Lack of sterility assurance: bag has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2021· Teligent Pharma, Inc.

Recalled Item: Lidocaine Hydrochloride Recalled by Teligent Pharma, Inc. Due to Superpotent...

The Issue: Superpotent Drug: Minimally superpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2021· Teligent Pharma, Inc.

Recalled Item: Lidocaine Hydrochloride Recalled by Teligent Pharma, Inc. Due to Superpotent...

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund