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.
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)
Reported Aug 20, 2014
Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Codman & Shurtleff, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Frederick Farms 4oz chocolate ice cream cups, net wt. 67grams, 24 per box, 231 boxes per pallet, expiration 6-10-15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Garber Ice Cream Company Inc.
FDA (openFDA food enforcement)
Reported Aug 20, 2014
Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1017. Product Usage: Used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Positioning Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 20, 2014
IntelliSpace Portal (ISP) DX/HX/EX, IntelliSpace Portal (ISP) IX, and IntelliSpace Portal (ISP) LX SPECT IntelliSpace…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Aug 13, 2014
Alcohol-Free Hand Sanitizer, 1. fl. oz. (30 ml) bottles capped with white sprayer, OTC, contains Benzalkonium chloride.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HLI dba Humphreyline Inc.
FDA (openFDA drug enforcement)
Reported Aug 13, 2014
Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Patient Data Manager 2.0 (Content manager 2.0, Patient Browser 4.0, DICOM Viewer 2.0) Brainlab Digital Lightbox. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
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.