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. 1,122 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,122 in last 12 months

Showing 7841–7860 of 53,829 recalls

DrugNovember 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2023· Padagis US LLC

Recalled Item: Trospium Chloride Extended-Release Capsules Recalled by Padagis US LLC Due...

The Issue: Failed Tablets/Capsules specifications; missing/broken/extra tablets within...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2023· Turncare, Inc

Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...

The Issue: A software issue where "low" and "terminal" battery alerts did not display...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ADLT BLOOD CULTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Polyethylene Glycol 400 Recalled by Cardinal...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lubricating Tears Eye Drops (Dextran/Hypromellose) Recalled by The Harvard...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by The Harvard Drug...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Propylene Glycol Recalled by Cardinal...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 31, 2023· BioReference Health, LLC

Recalled Item: The 4Kscore Test Recalled by BioReference Health, LLC Due to Mathematical...

The Issue: Mathematical modeling of the 4Kscore with and without DRE information was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing