Product Recalls in District of Columbia

Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,629 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,629 in last 12 months

Showing 53615380 of 13,355 recalls

DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Assorted IRC Display Recalled by Medtech Products, Inc. Due to...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Redness and Itchy Eye Relief Sidekick Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Hand Pocket Pal Tray Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Redness Relief Club Pack Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Club Pack Display Recalled by Medtech Products,...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Mometasone Furoate Cream USP Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: GMP Deviations: Glenmark received complaints stating that mometasone fuorate...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2019· Dercher Enterprises, Inc., DBA Gordon Laboratories

Recalled Item: MONSEL'S (Ferric Subsulfate) Solution Recalled by Dercher Enterprises, Inc.,...

The Issue: Microbial Contamination of Non-Sterile Products and Superpotent Drug: FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP Recalled by Lupin...

The Issue: Presence of Foreign Tablets/Capsules: Product complaint received of one...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...

The Issue: Lack of Assurance of Sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC Recalled by...

The Issue: Presence of Foreign Tablet/Capsule; one Promethazine tablet was found in a...

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

Class III — Low RiskOngoing
Refund
DrugJuly 17, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream USP100 Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out-of-specification result...

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

Class III — Low RiskOngoing
Refund
DrugJuly 17, 2019· Macleods Pharma Usa Inc

Recalled Item: Tamsulosin Hydrochloride Capsules Recalled by Macleods Pharma Usa Inc Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

Recalled Item: Timolol- Dorzolamide- Latanoprost P-F (0.5/2.0/0.005%) ophthalmic drops...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

Recalled Item: Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund