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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 Oct 23, 2019

Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…

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

ICU Medical Inc.

21 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2019

Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502

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

Roche Diagnostics Operations, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2019

L5C4531 X1 Integrated APD Set with Cassette 3-Prong Sterile, nonpyrogenic fluid path. Sterilized by ethylene oxide.

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2019

TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog # 5541-A-201 - Product Usage: Triathlon Femoral Distal…

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

Howmedica Osteonics Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Medfusion¿ Model 4000 Syringe Infusion Pump, with PharmGuard¿ Server Software (PGS). Sold under the following names:…

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2019

Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Allergan PLC

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2019

PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can

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

Natures One Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2019

XP- CR Tibial Tray- Interlok 59mm Item # 195268

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

Zimmer Biomet, Inc.

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Catalog Number 11403012

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

Angiodynamics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Norm-O-Temp model 111Z

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

Cincinnati Sub-Zero Products LLC, a Gentherm Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2019

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…

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

Bard Peripheral Vascular Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 4, 2019

PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane…

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

PreGel America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 28, 2019

ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 21, 2019

Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…

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

BIMBO Bakeries USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 21, 2019

Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810

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

Zimmer Biomet, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,…

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

Ideal Implant Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product Usage: The brushes are used to help clean out the…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2019

Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29 oz. Keep frozen, 7 pcs. UPC 074410925246 Distributed by…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Wismettac Asian Foods, Inc.

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2019

Maximum Pelvic Trainer (MPT)

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

Ralston Group

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2019

Truly Good Foods Edamame Beans Roasted and Salted 7 oz. (198g) plastic clam shell DISTRIBUTED BY TRULY GOOD FOODS,…

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

Tropical Nut & Fruit Company

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2019

Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

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Other states

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.