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.
4,062 stored notices name Maryland, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Mar 4, 2015
CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Echostar Spica 1.5T MRI system, for magnetic resonance imaging of the body.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alltech Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Cold Therapy Pad - cold water circulating pad, one unit per package. The pads are used to provide a patient with local…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Feb 18, 2015
The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corporation
FDA (openFDA device enforcement)
Reported Feb 18, 2015
MorningStar Farms Spicy Black Bean Burger: 9.50 oz (4 ct) - UPC 2898939207; 18.90 oz (8 ct): UPC 2898971750; 8.7 lb…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2015
Ground Cumin Seeds, ETO Treated, 50 lbs packaged in 50 lb brown paper bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Schiff Foods Products
FDA (openFDA food enforcement)
Reported Feb 18, 2015
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Craniomaxillofacial Division
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2015
System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings provide a sterile enclosure for the Stryker Non-sterile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2015
Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Virtual Imaging, Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Dried Bean Curd Satay Flavor, 24x150g, Item No. 8533.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gemini Food Corporation Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 11, 2015
ABL90 FLEX analyzer; Model number 393-090. A portable, automated analyzer that measures pH, blood gases, electrolytes,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Arriba! 16 oz. Chili Con Queso-Hot; 6 units per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Riba Foods Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 11, 2015
MobileDiagnost wDR motorized portable diagnostic X-ray systems.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal S.A.
FDA (openFDA device enforcement)
Reported Feb 10, 2015
Whole Foods Markets, Inc. Retira Productos Debido A Un Posible Error De Rotulacin Y A Un Alrgeno No Declarado
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Jan 29, 2015
California Firm Recalls Chicken Stew Products Produced Without Benefit of Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.California Firm
USDA FSIS
Reported Jan 28, 2015
FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aptalis Pharmatech Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Clear 1 lb packages of Natto Soybean Sprouts. These products are labeled as produced by Henrys Farm Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Henrys Farm Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 21, 2015
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia US Inc.
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.