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 48,122 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Mar 15, 2017
Trader Joes Imported English Authentic Lemon Curd, 10.5oz (300g), 24 jars/case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trader Joes Company
FDA (openFDA food enforcement)
Reported Mar 15, 2017
Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
BD AffirM VPIII Microbial Identification Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
McKesson Radiology 12.2 - Picture Archive Communication System (PACS)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Imaging
FDA (openFDA device enforcement)
Reported Mar 8, 2017
DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
123 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Feb 28, 2017
Wayne Farms, LLC Recalls Ready-To-Eat Chicken Products Due To Potential Processing Deviation
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wayne Farms LLC
USDA FSIS
Reported Feb 24, 2017
Fsis Issues Public Health Alert for Meat and Poultry Wraps Due to Possible Listeria Contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.JLM Manufacturing
USDA FSIS
Reported Feb 22, 2017
SLIMFIT X capsules, packaged in a 60-cont bottle
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jersey Shore Supplements, LLC
FDA (openFDA drug enforcement)
Reported Feb 22, 2017
Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 22, 2017
BrightView XCT
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 Feb 22, 2017
LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Whole Foods Market, TART FRESH FRUIT AMERO SHELL LARGE
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market Brand 365, LLC
7 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 15, 2017
Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labels: (a) angiodynamics…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
FDA (openFDA device enforcement)
Reported Feb 15, 2017
AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Cappuccino Snack Mix Lot code: 20161027; Best By: 05/25/17 Net Wt: 10 lb (2-5lb bags)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dutch Valley Food Distributors Inc.
FDA (openFDA food enforcement)
Reported Feb 15, 2017
Bariatric Bed - BAR600IVC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
2 more products in this recall
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.