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 60216040 of 13,355 recalls

DrugFebruary 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 10 Units added to NS 1000 mL (oxytocin and Recalled by Advanced...

The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Moisturizing Gel Hand Sanitizer (Ethyl Alcohol 62%) Recalled by Ecolab Inc...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%) Recalled by Ecolab Inc...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 30 Units added to NS 500 mL (oxytocin and Recalled by Advanced...

The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 20 Units added to NS 1000 mL (oxytocin and Recalled by Advanced...

The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Advanced Gel Hand Sanitizer (Ethyl alcohol 62%) Recalled by Ecolab Inc Due...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Express Gel Hand Sanitizer (Ethyl Alcohol 70%) Recalled by Ecolab Inc Due to...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Gel Hand Sanitizer (Ethyl Alcohol 70%) Recalled by Ecolab Inc Due to...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules USP Recalled by Dr. Reddy's...

The Issue: Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain brown...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 4, 2019· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2019· Akorn Inc

Recalled Item: Moisturizing Lubricant Eye Drops Recalled by Akorn Inc Due to Failed...

The Issue: Failed Stability Specification: out of specification results for Sodium...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 1, 2019· Mylan Institutional Inc

Recalled Item: Levoleucovorin Injection Recalled by Mylan Institutional Inc Due to Presence...

The Issue: Presence of Particulate Matter: particulate matter identified as copper salts

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray...

The Issue: Defective Container: Potential for broken glass in the neck area of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications: Out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Diltiazem HCl CD capsules Recalled by Valeant Pharmaceuticals North America...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2019· US Compounding Inc

Recalled Item: Ephedrine Sulfate Recalled by US Compounding Inc Due to Lack of assurance of...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund