All recall categories

Recalls distributed in Maryland

These notices name Maryland 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.

4,005 stored notices name Maryland, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,132 notices were distributed nationwide, so they reach Maryland too — those are in the archive.

Medical devices

Reported Aug 21, 2013

1) Adult Manual Resuscitator, 2K8004, Oxygen Reservoir Bag, Adult Mask; 2) Adult Manual Resuscitator, 2K8005, 40" (1.0…

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

Carefusion 2200 Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2013

epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing of samples for pH, pCO2, pO2, Sodium…

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

Epocal

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2013

GE LightSpeed CT750 HD The GE LightSpeed CT750 HD Computed Tomography X-ray system is intended to produce…

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

GE Healthcare, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 21, 2013

RYBACKA WIES brand HERRING FILLETS IN OIL (MATJES SLEDZ W OLEJU), Net Wt. 17.6 oz. (500g), UPC 0 21143 24122 8,…

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

Gold Star Smoked Fish Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 21, 2013

Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375, 2) 6801890, 3) 6802445, 4) 6802413 Product…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2013

Remel X/pect Flu A&B Control Swabs, For In Vitro Diagnostic Use, Ref R246003, each package contains 20 Flu A Control…

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2013

ADVIA Centaur Calibrator A. Cat. #04800735, SMN 10285904 (6 pack); Cat. # 04800840, SMN 10285905 (6 pack - REF). For…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2013

Siemens AXIOM Artis zeego x-ray, angiographic system

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)

Medical devices

Reported Aug 14, 2013

Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and…

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

MRidium 1145 Dose Reduction System (DERS) drug library kit. (This is an option for the MRidium 3860+MR Infusion Pump…

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

Iradimed Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

Nestle Nutrition, Compat, Enteral Feeding Tube, sterile, 8 French (REF 08310400), 10 French (REF 08310600), and 12…

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

Nestle HealthCare Nutrition

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2013

Earth's Pride Organics: Organic Oregano, 2.2 oz. Packaged at 12 units per case. Packaged in a glass jar with cork…

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

Olde Thompson, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 14, 2013

TCM4 series Base Units, and spare part Power Supply, Radiometer Medical ApS, Akandevej 21, Br¿nsh¿j, Denmark,…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL (DC107) Product Usage: The TACR method is an…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole) Product Usage: The Sonopet Console is indicated…

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

Stryker Instruments Div.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2013

Raw Pistachio Halves, 1 pound bag. Item Number 11910, UPC Code: 172043119107; Raw Pistachio Halves, 4 pound bag. Item…

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

Superior Nut Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2013

GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. The device is a general purpose ultrasound…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)

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

HeartWare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals,…

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

Hospira Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient…

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

Picis Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

AIA Analyzer Pipette Tips used on Tosoh AIA-2000, AIA-1800, AIA-900 and AIA-600II Analyzers, 1000 tips/bag AIA-Analyzer…

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

Tosoh Smd Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2013

Pimento Cheese, packaged in 7 oz. plastic containers, and labeled in part ***Made by Whole Foods Market, Landover, MD…

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

Whole Foods Market Mid-Atlantic Kitchen

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2013

Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making…

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

Advanced Orthogonal Equipment, Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

Sodium Bicarbonate, USP Provided bulk as raw material - label not applicable according to firm Dialysis Grade 1.5…

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

Church & Dwight 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.