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 Nov 30, 2016
ACTIS Flex Reamers SZ 0/1; 2/3; 4/5; 6/7; 8/9; 10/11; 12, Product is sold non-sterile, these instruments are packed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Depuy Orthopaedics Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Philips Healthcare System X-ray Tomography Computed :
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCain Foods USA
FDA (openFDA food enforcement)
Reported Nov 23, 2016
OMNIBotics Tracker Kit -Model: RM-10000 The TOTAL KNEE SURGETICS Navigation System with iBlock (Now OMNIBotics) is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Omni Life Science
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 22, 2016
Hale And Hearty Soups, LLC Retira Sopa De Pollo Al Estilo Chile Lista Para Comer Debido A Una Posible Contaminacin Con…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hearty Acquisitions, LLC
USDA FSIS
Reported Nov 18, 2016
Wayne Farms, LLC Retira Productos De Pechuga De Pollo Listos Para Comer Los Cuales Podran Estar Medios Crudos
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Nov 16, 2016
Fruit 66 Mixed Berry, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.1 Epic, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 16, 2016
AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Koffee Kup Potatoe Hamburger Buns, Plain and Seeded, 8 pk
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Koffee Kup Bakery Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 16, 2016
TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a medical device software that is installed on bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medimaps Group
FDA (openFDA device enforcement)
Reported Nov 16, 2016
FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended for use in the cardiovascular system for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SentreHeart Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
The Stone Ground Peanut Butter Chocolate Bar, Net wt. 2.5 oz. UPC 8 55966 00107 9.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jjbl LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 9, 2016
BELGIAN BOYS MINI PANCAKES, NET WT. 10.6 oz (300g), 36 Count, UPC 857290005204, Product of The Netherlands --- Produced…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Le Petit Belge
FDA (openFDA food enforcement)
Reported Nov 9, 2016
Rigid Suction Canister 3000 CC and 2000 CC.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Select Recipe Buttermilk Ranch Dressing, Net contents: 1 GAL (3.79 L), 4 X 1 GAL
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Oasis Foods Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 9, 2016
Hollandaise Sauce, sold as Sallere Classic Sauces and Butters, refrigerated product. Each plastic tub has a net wt 7…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Rikki USA, Inc.
FDA (openFDA food enforcement)
Reported Nov 2, 2016
PhoenixSpec Calibrator & Kit is used to calibrate the PhoenixSpec & Phoenix AP Instruments. The instruments are then…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 2, 2016
4205 Journey Rolling Walker Product Usage: used to assist people in walking
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sequent Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US, ex-tem. Used to monitor the coagulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
FDA (openFDA food 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.