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 Mar 20, 2013
Mochiko Blue Star Sweet Rice Flour, Net Wt 50 lb. or packaged in 1 lb bags. Koda Farms Milling, Inc. South Dos Palos,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Koda Farms Inc.
FDA (openFDA food enforcement)
Reported Mar 20, 2013
Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers : 515-015400 for the 32 channel amplifier and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Incorporated
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Brilliance 6, 10, 16, 40, 64, Big Bore and the iCT, iCT SP, Ingenuity CT and MX8000 Dual v. EXP are Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 20, 2013
365 Organic Orzo, 16oz, 20 carton/case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 13, 2013
Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For temporary (<30 days) use with recording,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ad-Tech Medical Instrument Corporation
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Atricure Inc., Max1 Isolator Transpolar Pen. Model A000163. Used to ablate cardiac tissues during cardiac surgery using…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atricure Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Deep Best Quality Dry Garlic Chutney (Thechaa); Net Wt. 4 OZ.; UPC 011433111201; Deep Foods, Inc. Union, NJ 07083
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Deep Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 13, 2013
PSX PROXIMATE Skin Staple Extractor, ETHICON ENDO-SURGERY, LLC. For routine skin closure in a wide variety of surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2013
GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume Viewer 3.x (Advantage Workstation 4.1) Volume…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Chocolate bridge mix in 10 oz, 3 oz, and 3.5 oz bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gorant Candies Inc. A Division
3 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 13, 2013
D3000 Advantage Drive System, 115v Product Usage: The Advantage Drive Systems function as a powered instrument system…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Linvatec Corp. dba ConMed Linvatec
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Philips Medical System Extended Brilliance Workspace (EBW), Computed Tomography X-Ray System. The Extended Brilliance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2013
AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and moisture-stable materials used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Synthes Multi-Vector Distractor Body, Part Number 487.931. For mandibular bone lengthening.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2013
GoldCoast Salads Blue Crab Spread (8oz and 16oz in flexible plastic cup with flexible plastic lids - keep refrigerate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GoldCoast Salads
3 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 6, 2013
Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by Philips Medical Systems, Highland Heights, OH…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Stryker XIA 3 Iliac Screwdriver, 3-PCS. The XIA 3 Iliac Screwdriver is used to drive XIA 3 closed head Monoaxial and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Animas Corporation
FDA (openFDA device enforcement)
Reported Feb 27, 2013
LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage…
High riskUsing this product could cause serious injury, illness or death — stop using it now.DePuy Orthopaedics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Feb 27, 2013
MAYFIELD¿ Composite Series Base Unit Standard, Model (A3101), Rx ONLY, Integra LifeScience Corporation, 4900 Charlemar…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Lean Cuisine Culinary Collection Mushroom Mezzaluna Ravioli ravioli filled with portobello & button mushrooms, romano &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA
FDA (openFDA food enforcement)
Reported Feb 27, 2013
Vascular Solutions, SuperCross Microcatheter, Sterilized using ethylene oxide, Rx Only, Model numbers 5300 - 5307,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, 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.