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 85418560 of 13,439 recalls

DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: DIPYRIDAMOLE Tablets USP Recalled by Boehringer Ingelheim Pharmaceuticals,...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Persantine (dipyridamole USP) tablets Recalled by Boehringer Ingelheim...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2016· Par Pharmaceutical, Inc.

Recalled Item: Travoprost Ophthalmic Solution USP Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Lack of Assurance of Sterility; damage to the internal portion of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2016· West-Ward Pharmaceutical

Recalled Item: PredniSONE Tablets USP Recalled by West-Ward Pharmaceutical Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2016· West-Ward Pharmaceuticals Corp.

Recalled Item: Phenobarbital Tablets Recalled by West-Ward Pharmaceuticals Corp. Due to...

The Issue: Failed Dissolution Specifications: Phenobarbital Tablets have an out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2016· Amerisource Health Services

Recalled Item: Paricalcitol Capsules Recalled by Amerisource Health Services Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: This repackaged product was...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: USCG Boat Response Kit - Product Code 80-0353 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Aid Backpack Kit - Product Code 85-0917 Recalled by North American Rescue...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 24 FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical,...

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Mini Resupply Trauma Kit - Product Code 85-0835 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: K-9 Trauma Field Kit - Product Code 80-0211 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Range Trauma Kit - Product Code 85-1274 Recalled by North American Rescue...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Amphibious Trauma Kit - Product Code 85-0639 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Advance Trauma Kit - Product Code 85-0742 Recalled by North American Rescue...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical,...

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess FE 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc....

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical, Inc....

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund