Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,848 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,848 in last 12 months

Showing 19011920 of 13,439 recalls

DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: oxyTOCIN 15 units added to 0.9% sodium chloride 250 mL per bag Recalled by...

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: Cardioplegia Solution Recalled by Central Admixture Pharmacy Services, Inc....

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: Cardioplegia Solution Recalled by Central Admixture Pharmacy Services, Inc....

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: Neonatal PN Starter Bag Recalled by Central Admixture Pharmacy Services,...

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: Cardioplegia Solution Recalled by Central Admixture Pharmacy Services, Inc....

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: oxyTOCIN 60 units added to 0.9% sodium chloride 1 Recalled by Central...

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: heparin added to 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: Modified del Nido Microplegia Recalled by Central Admixture Pharmacy...

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: dilTIAZem added to 0.9% sodium chloride Recalled by Central Admixture...

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...

The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 27, 2023· Teva Pharmaceuticals USA Inc

Recalled Item: Fentanyl Buccal Tablets CII Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
DrugApril 27, 2023· Teva Pharmaceuticals USA Inc

Recalled Item: Fentanyl Buccal Tablets CII Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
DrugApril 27, 2023· Teva Pharmaceuticals USA Inc

Recalled Item: Fentanyl Buccal Tablets CII Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
DrugApril 27, 2023· Teva Pharmaceuticals USA Inc

Recalled Item: Fentanyl Buccal Tablets CII Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
DrugApril 27, 2023· Teva Pharmaceuticals USA Inc

Recalled Item: Fentanyl Buccal Tablets CII Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Levofloxacin Injection 500mg/20 mL (25 mg/mL) Recalled by Akorn, Inc. Due to...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Clobetasol Propionate Cream Recalled by Akorn, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Levofloxacin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Tropicamide Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Calcitriol Injection 1 mcg/mL Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund