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. 2,807 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,807 in last 12 months

Showing 87018720 of 13,439 recalls

DrugAugust 24, 2016· Sandoz Inc

Recalled Item: Phenylephrine HCI Injection Recalled by Sandoz Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2016· Impax Laboratories, Inc.

Recalled Item: Lamotrigine Orally Disintegrating Tablets (ODT) Recalled by Impax...

The Issue: Labeling; Label Mixup; box labeled to contain 200 mg blister packs but...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 19, 2016· Unichem Pharmaceuticals Usa Inc

Recalled Item: Lamotrigine Tablets Recalled by Unichem Pharmaceuticals Usa Inc Due to...

The Issue: Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the...

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

Class III — Low RiskOngoing
Refund
DrugAugust 18, 2016· West-Ward Pharmaceuticals Corp.

Recalled Item: Amoxicillin For Oral Suspension Recalled by West-Ward Pharmaceuticals Corp....

The Issue: Labeling: Label Error on Declared Strength- bottles missing colored coded...

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

Class III — Low RiskOngoing
Refund
DrugAugust 16, 2016· Sperian Eye & Face Protection, Inc

Recalled Item: Honeywell eyesaline Eyewash Sterile Isotonic Solution Recalled by Sperian...

The Issue: Non Sterility; contaminated with Klebsiella pneumoniae

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 15, 2016· Hospira Inc.

Recalled Item: DOBUTamine Injection Recalled by Hospira Inc. Due to Discoloration: Firm...

The Issue: Discoloration: Firm received complaints of product discoloration and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2016· Allergy Laboratories, Inc.

Recalled Item: Ephedrine Sulfate Injection Recalled by Allergy Laboratories, Inc. Due to...

The Issue: Lack of Assurance of Sterility: An FDA inspection at the facility raised...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid Recalled by...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Diocto Syrup (docusate sodium) Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Sennazon (sennosides) Syrup Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Aller-Chlor (chlorpheniramine maleate) Syrup Recalled by Pharmatech LLC Due...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senexon Liquid (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof-A (acetaminophen Recalled by Pharmatech LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senna Syrup (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2016· Teva North America

Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2016· Genzyme Corporation / Genzyme Biosurgery

Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund