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 20, 2019
Finax Muesli with Nuts and fruit 22.9-oz. Heat sealed plastic bag; 10 bags/case UPC: 7311142201402
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chicago Importing Co.
FDA (openFDA food enforcement)
Reported Mar 20, 2019
Oxygen, Refrigerated Liquid USP, Rx only, cylinder, a) Roberts Home Medical, Inc. Rockville MD 20855, b) Roberts Home…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roberts Home Medical LLC
FDA (openFDA drug enforcement)
Reported Mar 20, 2019
AMSCO 3000 Series Washer/Disinfector Model # 3052
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 13, 2019
DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kingston Pharma LLC
FDA (openFDA food enforcement)
Reported Mar 13, 2019
Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
C2 CryoBalloon Controller, REF: FG-1017, with Controller Software v1.18.258 The C2 CryoBalloon Ablation System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Mar 13, 2019
Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rvo 2.0, Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Phoenix AST-s Indicator, Catalog Number 246009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Craft Granola Goldenola Turmeric & Ginger, packaged in 3 oz. and 11 oz. poly bag, UPC: 860157002028 and 8601570020135
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Birdseed Food Co. LLC
FDA (openFDA food enforcement)
Reported Mar 6, 2019
Equinoxe Preserve Humeral Stem, 8mm Product Usage: The Equinoxe Preserve Stems are indicated for use in skeletally…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Orchards
FDA (openFDA food enforcement)
Reported Mar 6, 2019
The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Puratos Corporation
FDA (openFDA food enforcement)
Reported Mar 6, 2019
Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet Spine Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chicago Bar Company LLC Rxbar
18 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products LLC, a Gentherm Company
FDA (openFDA device enforcement)
Reported Feb 20, 2019
MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2019
ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Barcelona Nut Company, Roasted and Salted Select Inshell Pistachios 21/25, flexible package, shelf life of one year.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Barcelona Nut Company
FDA (openFDA food enforcement)
Reported Feb 13, 2019
BD FACSLyric 3L 10C with FACSuite Clinical Software v1.1.1, catalog number 662878 BD FACSLyric is a high-performance…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
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Other states
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.