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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,411 in last 12 months

Showing 3922139240 of 47,654 recalls

DrugNovember 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful BEE POLLEN Recalled by Enterprises, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful INFINITY Recalled by Enterprises, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 31, 2014· Accuray Incorporated

Recalled Item: CyberKnife Robotic Radiosurgery System with the first generation IRIS...

The Issue: Software upgrade to correct potential safety issue related to CyberKnife...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2014· Alcon Research, Ltd.

Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....

The Issue: Alcon is conducting a medical device recall due to the possible presence of...

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

Class II — Potential Health HazardOngoing
DrugOctober 30, 2014· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Subpotent Drug: Heparin raw material was found to have low potency

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2014· Respironics California Inc

Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...

The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Inspiration system: Product Usage: mammography exams Recalled by...

The Issue: It was determined that if the Mammomat Inspiration system is not secured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2014· Cooper Vision Caribbean Corp.

Recalled Item: Soft Contact Lens Recalled by Cooper Vision Caribbean Corp. Due to Portions...

The Issue: Portions of the lots may contain units with an incorrect lens axis condition.

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

Class II — Potential Health HazardOngoing
FoodOctober 28, 2014· Marathon Ventures Inc

Recalled Item: Macadamia nuts in various formats: (1.) Western Family Macadamia Diced Nuts...

The Issue: Macadamia nuts may have possible contamination with Salmonella florida.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 27, 2014· Kent Precision Foods Group, Inc.

Recalled Item: Chicken flavored broth base and seasoning Recalled by Kent Precision Foods...

The Issue: Orrington Farms Chicken Flavored Broth Base & Seasoning, Low Sodium labels...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2014· Straumann USA, LLC

Recalled Item: Drill set long Recalled by Straumann USA, LLC Due to Drill set may contain...

The Issue: Drill set may contain incorrect drill.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2014· ArthroCare Medical Corporation

Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...

The Issue: Potential breach of sterile barrier due to defective product tray.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2014· CooperSurgical, Inc.

Recalled Item: CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D Recalled by...

The Issue: Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2014· Discus Dental LLC

Recalled Item: Relief ACP Oral Care Gel intended to relieve discomfort from Recalled by...

The Issue: Product sold after April 1, 2014 were inadvertently filled with hydrogen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2014· AGFA Healthcare Corp.

Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some...

The Issue: Some material of the coating Type CXCPMV3 has potential artifacts showing a...

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

Class III — Low RiskOngoing
Medical DeviceOctober 24, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Titan Reverse Shoulder System right and left head cutting templates...

The Issue: A single lot of left and a single lot of right Reverse Shoulder System...

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

Class II — Potential Health HazardOngoing
DrugOctober 24, 2014· Hospira Inc.

Recalled Item: Meropenem I.V. 1 g is supplied in 30 mL injection vials Recalled by Hospira...

The Issue: Defective Container: Glass vials may crack due to low (thin) out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2014· CareFusion 213, LLC

Recalled Item: Scrub Care Chlorhexidine Gluconate Solution Recalled by CareFusion 213, LLC...

The Issue: Does Not Meet Monograph: Chlorhexidine Gluconate Surgical Scrub Brush is...

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

Class III — Low RiskOngoing
Refund
FoodOctober 23, 2014· Coca-Cola Company (The)

Recalled Item: Odwalla Vanilla Almondo Protein Recalled by Coca-Cola Company (The) Due to...

The Issue: There is the potential that some of the bottles could exhibit spoilage...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 23, 2014· Coca-Cola Company (The)

Recalled Item: Odwalla Chocolate Protein Shake Recalled by Coca-Cola Company (The) Due to...

The Issue: There is the potential that some of the bottles could exhibit spoilage...

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

Class II — Potential Health HazardOngoing
Refund