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. A further 48,853 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Sep 18, 2013
ADVIA Centaur Folate (100 Tests), SMN 10310308, Cat No. 06367974 In vitro diagnostic use in the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2013
Boston Scientific, Small Peripheral Cutting BalloonTM, Sterilized using irradiation: The Peripheral Cutting Balloon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2013
CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT, Product Code: 2839-05-000 The CONFIDENCE Spinal Cement System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2013
Chocolate covered raisinsin 4 oz flexible bags labeled in part "***Pennsylvania Dutch Candies***Chocolate Covered…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Warrell Corporation
FDA (openFDA food enforcement)
Reported Sep 4, 2013
Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico MIS Posterior Fixation System is intended to facilitate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
DeRoyal Insufflation Tubing sets: 1) REF 28-0206 Insufflation Tubing, Laparoscopic Rx Only 2) REF 28-0214 Hi-Flow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Technologies Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat. #CT0036B, packaged in cartridges of 50 discs,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Remel Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Synthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Torque limiting attachment, 1.2Nm Synthes VA-LCP Distal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Aug 28, 2013
GYRUS ACMI, REF 3740, Everest BiCOAG Bipolar Dissecting Forceps 5mm/45 cm, Sterile EO. GYRUS ACMI, REF 3740PK, or REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gyrus Medical, Inc.
FDA (openFDA device enforcement)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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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.