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Recalls distributed in District of Columbia

These notices name District of Columbia in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

1,461 stored notices name District of Columbia, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach District of Columbia too — those are in the archive.

Medical devices

Reported Dec 24, 2014

Additional devices identified in new FSN MA-FCO 83000190: QLAB versions 10.0 with a2DQ and/or aCMQ plug-ins installed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 17, 2014

Margaret Holmes Mixed Greens 14.5 oz, Distributed by McCall Farms, Effingham, SC

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Mccall Farms Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2014

BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2014

Amerigel Hydrogel Wound Dressing Wound management

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amerx Health Care Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

Abbott m2000sp, an automated system for performing sample preparation for nucleic acid testing.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Molecular

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2014

CyberKnife Robotic Radiosurgery System with the first generation IRIS Variable Aperture Collimator. The CyberKnife is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Accuray Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2014

Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Biomerieux

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2014

GE Healthcare Infinia (including Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye, Infinia II Hawkeye 4,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2014

The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Steris Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 19, 2014

365 Organic Raisin Granola in 17 ounce (482 gram) cardboard cartons; 12 cartons per case. UPC: 099482448738

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Whole Foods Market Brand 365, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 12, 2014

Thyroglobulin (1D4) is a mouse anti-human monoclonal antibody produced as a tissue culture supernatant, and supplied in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 5, 2014

DMI Duro-Med Industries Rollator Transport Chair; Wheel Size: 7 1/4"; Overall Width: 23 1/2"; Seat Height: 21 1/4";…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Briggs Medical Service Company d.b.a. Mabis

FDA (openFDA device enforcement)

Food

Reported Nov 5, 2014

Family Gourmet Long Grain Enriched White Rice in 32 oz. clear plastic bags (SKU: 1218898) and 80 oz. clear plastic bag…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Family Dollar Stores - NC Distribution Center

FDA (openFDA food enforcement)

Medical devices

Reported Oct 29, 2014

Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage: They are indicated for use in adult &…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mortara Instrument, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 29, 2014

Symbia E is a multi-purpose SPECT system ideal for hospitals and outpatient centers. It is used to detect or image the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Oct 24, 2014

New Jersey Firm Recalls Salad with Chicken Due To Misbranding and Undeclared Allergen

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Taylor Farms New Jersey, Inc.

USDA FSIS

Medical devices

Reported Oct 22, 2014

Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arjo, Inc. dba ArjoHuntleigh

FDA (openFDA device enforcement)

Medical devices

Reported Oct 15, 2014

GE Healthcare Carescape Patient Data Module

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 15, 2014

Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nemschoff Chairs, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2014

The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 1, 2014

Product is packaged in a cardboard box and labeled in part, "SOUTHERN HOME Mozzarella Sticks***CONTAINS: WHEY, MILK,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Great American Appetizers, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 24, 2014

Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amerx Health Care Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.