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.
4,064 stored notices name Maryland, reported between Jun 20, 2012 and Nov 18, 2026.
Reported Jan 2, 2013
Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjo, Inc. dba ArjoHuntleigh
FDA (openFDA device enforcement)
Reported Jan 2, 2013
GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece Neonatal Patient Circuit Kit Disposable with Size…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jan 2, 2013
Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog no. D140010, Large Curve catalog no.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greatbatch Medical
FDA (openFDA device enforcement)
Reported Jan 2, 2013
Zimmer Spine Ardis Inserter, Rx, non-sterile
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Dec 26, 2012
MAYFIELD Composite Series Base Unit, Model A3101, a Swivel Adaptor (A3018) is an integral component of the Base Unit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 26, 2012
Invacare Height Adjustable (walking) Canes, Model Numbers: 8916, 8917, and 40918-6. The device is packaged six (6)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Dec 26, 2012
ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ThyssenKrupp Access Corp.
FDA (openFDA device enforcement)
Reported Dec 26, 2012
Dried Apricots 6 oz UPC 7203670494
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Alternatives LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 19, 2012
Baugher's Apple Cider, one gallon and half gallon plastic jugs, with plastic caps labeled in part ***Fresh***…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baugher Enterprises, Incorporated
FDA (openFDA food enforcement)
Reported Dec 19, 2012
Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular whole bean coffee packaged in the following sizes: 12…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Berres Brothers, Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 19, 2012
WANG Transbronchial Aspiration Needles Cat. No. MW-222, WANG Cytology Needles, Central or Peripheral Regions, 22 g x 13…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
Novocastra Ready-to-Use Mouse Monoclonal Antibody Terminal Deoxynuceotidyl Transferase Staining Reagent; an in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Dec 19, 2012
Baby Quasar (LAB-001-D, BQ101) and Baby Quasar Pink (LAB-046-A BQ101-P) are infrared LED lamps that are labeled in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quasar Bio-Tech, Inc. dba Silver Bay LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Cobas 8000 Modular Analyzer Series, Model/Catalog/Part Number: 05641489001. The Cobas 8000 is a fully automated system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Echo Bi-Metric Press-Fit Stems/Echo Bi-Metric 11mm x 135mm Collarless Porous Stem (Orthopedic Implant) Indications: 1)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Ground Hot Pepper Chillies, 5 oz. plastic jars, 24 jars/case; jars labeled in part ***Imported and distributed by Nina…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ernimich, Inc. (dba Nina International, Inc.)
FDA (openFDA food enforcement)
Reported Dec 5, 2012
IO FiX X-Post Reamer, Extremity Medical, www.extremitymedical.com; Customer Service: 888.499.0079 The X-Post Reamer is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Jimmy Dean French Toast & Sausage Sandwich, Net Wt 3.9 oz (110g); a food service individually butcher paper wrapped,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hillshire Brands Company
FDA (openFDA food enforcement)
Reported Dec 5, 2012
The brand name is MRidium Series 1000 MR Infusion Sets, Type 1058 MR IV Extension Set, Lot Code LBG001. The generic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Iradimed Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
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.