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 Nov 13, 2013
DRX Revolution, Catalog #'s 1)1019397, 2) 1023415 (w/ installation warranty, US-only) and 3) 1023423 (w/ parts…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids, or in various kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Giant Eagle Candy Place Candy Corn Mix in a clear plastic container, net wt. 13 oz, Distributed by Giant Eagle Inc.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Eagle, Inc.
FDA (openFDA food enforcement)
Reported Nov 13, 2013
MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25- gauge illuminator for vitreo-retinal surgery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Insight Instruments, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Jim Dandy¿ Iron Fortified Quick Grits, 1lb paper box, Labeled in part "INGREDIENTS: IRON, WHITE CORN GRITS, NIACIN,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J M Smucker Co.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2013
Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen the abdominal muscles.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pinook-Usa
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes; Vaporization electrode, sterite; 4mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf Medical Instruments Corp.
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Angel Food Cake; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Safeway Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2013
ADVIA Centaur Intact PTH Calibrator (6 pack); Catalog Number: SMN 10492387 For in vitro diagnostic use in calibrating…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2013
GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 5, LEFT, QTY: (1), REF 71420168. Product Usage: orthopaedic
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre; 15248C-22/25 The Regional Anesthesia family of products is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
S5 Heart-lung machine, Stockert S5 System. Catalogue No: 48-30/40/50-00. The Stockert S5 System is intended to be used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group Deutschland GmbH
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Harmony Equipment Management System, Model #603X/80XX, STERIS Corporation, Mentor, OH Harmony Equipment Management…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Nov 13, 2013
VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150 tablets glass, amber…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitalab Co. Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2013
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Atossa Genetics, Inc.
FDA (openFDA device enforcement)
Reported Nov 6, 2013
P.F. Chang's Home Menu, Pork & Leek Dumplings, frozen, packaged in 12.5 oz bags. UPC: 0 36200 21215 8
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2013
Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2013
PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
St. Marcellin Au lait pasteurise fabrique en Dauphine l'unite: poids net 80ge Fromagerie Qurtet 38470 VINAY
High riskUsing this product could cause serious injury, illness or death — stop using it now.Epicure Food Corp.
FDA (openFDA food enforcement)
Reported Nov 6, 2013
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare It
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
MAQUET Getinge Group CARDIOHELP Base Unit REF 70104.7999 REF 70104.8012 Manufactured for: MAQUET Cardiopulmonary AG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Nov 6, 2013
PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower G.I. Endoscopes are provided with Air/Water…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pentax Medical Company
FDA (openFDA device enforcement)
Reported Nov 6, 2013
Breeze C Scooter is a motorized electric scooter for elderly people. Brand name Breeze, model C. It is intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.S.a.e. Afikim
FDA (openFDA device enforcement)
Reported Oct 30, 2013
NatureMost LABORATORIES NATURAL WHEY POWER W / YERBA MATE VANILLA / ALMOND Dietary Supplement NET WEIGHT 3 LBS.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.NatureMost
1 more product in this recall
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.