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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,395 in last 12 months

Showing 4302143040 of 47,654 recalls

Medical DeviceJuly 22, 2013· Synthes USA HQ, Inc.

Recalled Item: 3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm Recalled by...

The Issue: All lots of 3.7mm and 5.0mm Dynamic Locking Screw (DLS) were recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· MCKESSON TECHNOLOGIES INC

Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...

The Issue: The firm issued a clinical alert after users reported an issue where the...

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

Class II — Potential Health HazardOngoing
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Siloutte Suplemento Alimenticio Recalled by Herbal Give Care Llc...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Te Recalled by Herbal Give Care Llc Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio Recalled by...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement Recalled by...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement 1500mg Recalled by Myson Corporation, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement Liquid Recalled by Myson Corporation, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Bracco Diagnostics Inc

Recalled Item: Tagitol V Barium Sulfate Suspension (40% w/v Recalled by Bracco Diagnostics...

The Issue: Failed Stability Specifications: Tagitol V Barium Sulfate Lot #65846 sampled...

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

Class III — Low RiskOngoing
Refund
DrugJuly 19, 2013· Watson Laboratories Inc

Recalled Item: Oxycodone and Acetaminophen Capsules Recalled by Watson Laboratories Inc Due...

The Issue: Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500...

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

Class III — Low RiskOngoing
Refund
FoodJuly 19, 2013· Plum Inc

Recalled Item: Plum Organics Mighty 4 Essential nutrition blend Recalled by Plum Inc Due to...

The Issue: Intermittent ineffective hermetic seal on pouch package leading to potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2013· Plum Inc

Recalled Item: Plum Organics Mighty 4 Essential nutrition blend Recalled by Plum Inc Due to...

The Issue: Intermittent ineffective hermetic seal on pouch package leading to potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2013· Plum Inc

Recalled Item: Plum Organics Mighty 4 Essential nutrition blend Recalled by Plum Inc Due to...

The Issue: Intermittent ineffective hermetic seal on pouch package leading to potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2013· Plum Inc

Recalled Item: Plum Organics Mighty 4 Essential nutrition blend Recalled by Plum Inc Due to...

The Issue: Intermittent ineffective hermetic seal on pouch package leading to potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2013· Plum Inc

Recalled Item: Plum Organics Mighty 4 Essential nutrition blend Recalled by Plum Inc Due to...

The Issue: Intermittent ineffective hermetic seal on pouch package leading to potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 19, 2013· Blue Belt Technologies MN

Recalled Item: Blue Belt Technologies Recalled by Blue Belt Technologies MN Due to Blue...

The Issue: Blue Belt Technologies is recalling sterile Monitor Drapes used with their...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR V-Patch Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Mesh (All Sizes Recalled by Atrium Medical Corporation Due to...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing