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 Sep 3, 2014
Rising Moon Organics Butternut Squash Ravioli, Organic, Vegetarian & Delicious; Keep Frozen; Net Wt. 8 oz. UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carmel Food Group, Inc.
FDA (openFDA food enforcement)
Reported Sep 3, 2014
CollectEVAC, Sterile device with tubing and adaptor for use with ACMI and STORZ/Wolf resectoscopes. Part number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Civco Medical Instruments Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2014
CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a Tyvek-film sterilizable outer package and is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2014
Cordis EMPIRA NC RX PTCA Dilatation Catheter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2014
McCormick Ground Oregano in 0.75 oz plastic bottle. UPC NUMBER: 52100003566 (as seen on label: 0-523561-6) MCCORMICK…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCormick & Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 3, 2014
Verigene CYP2C19 Nucleic Acid Test (CYP2C19 Test). Each CYP2C19 kit consists of 20 Verigene CYP2C19 Nucleic Acid Test…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nanosphere, Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2014
Midazolam HCl 2 mg/ml in 0.9% Sodium Chloride in 30 mL PVC Vial, Rx Only. Pharmakon Pharmaceuticals, Inc., 14450 Getz…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pharmakon Pharmaceuticals
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 3, 2014
Shoprite Spring Water Net 1 GAL (120 Fl Oz.) 3.78L Distributed by Wakefern Food Corp Elizabeth, NJ Made in USA UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Readington Farms Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 3, 2014
4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy, LDS 15mm Conn Pediatric Endotracheal Intubation Kit
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smiths Medical ASD, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2014
American Spoon Food Sour Cherry Marmalade, 9.5 oz in glass jars with metal lid e. Total package size (e.g. 12 packages…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Spoon Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 27, 2014
Vanguard 360 Femoral Boss Reamer, Label: REF 32-488474 VANGUARD 360 1NSTRUMENT FEMORAL BOSS REAMER NON-STERILE, BIOMET…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
GE Healthcare, Discovery XR656P/N 5374989/5397837 is intended to generate digital radiographic images of the skull,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Gyrus ACMI Falope-Ring Dilator, item 000878-4. The Falope-Ring Dilator is a conical plastic device that is a component…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gyrus Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
All brochures printed before November 20, 2013 for the HyperBlue 1530 medical laser, including the product brochure and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hyperion Medical
FDA (openFDA device enforcement)
Reported Aug 27, 2014
CAP Change Kit w/MicroClave Clear, Item No. B78109 BD prefilled syringes are co-packaged into a kit with ICU devices…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and device controller for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Product is in a 160 gram, light green tin container, labeled in part: "ecoato Sweet Paprika Powder Product of Spain"
High riskUsing this product could cause serious injury, illness or death — stop using it now.The TJX Companies, Inc.
FDA (openFDA food enforcement)
Reported Aug 27, 2014
TomoTherapy Treatment System, Model: Hi-Art, Catalog/Part Number: H-0000-0003, software versions 1.2.0, 1.2.1 and 1.2.2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TomoTherapy Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a TERUMO company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascutek, Ltd.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
BD Multi Check CD4 Low Control Catalog No. 340916 is intended as a complete process control for immunophenotyping by…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.BD Biosciences, Systems & Reagents
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Device Brand Name: Distal Radius Fracture Repair System Device Classification Name: Plate, Fixation, Bone Device Common…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosound Esaote, Inc.
FDA (openFDA device enforcement)
Reported Aug 20, 2014
CSI Cardiovascular Systems, Inc., Diamondback 360 Peripheral Orbital Atherectomy System, Model Number DBP-125MICRO145,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardiovascular Systems, 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.