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 48,100 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Nov 27, 2019
Dry dates packaged under the following brands: Keshav Dry Yellow Dates, 7oz., UPC: 643864233124 and 14oz., UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peekay International, Inc.
FDA (openFDA food enforcement)
Reported Nov 27, 2019
Randox Liquid Cardiac Controls Catalogue Number CQ5051
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories, Limited
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 22, 2019
Ajinomoto Foods North America, Inc. Retira Productos De Arroz Frito Con Pollo Debido A Una Posible Contaminación Con…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ajinomoto Foods North America
USDA FSIS
Reported Nov 21, 2019
Missa Bay, LLC Recalls Salad Products Due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Missa Bay LLC
USDA FSIS
Reported Nov 20, 2019
CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit. 2 units per case The devices could…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2019
2000 Vascular with 30 Degree option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
ORTHOFIX Catalogue Number: ref 11007, drill bit diameter 4.8 MM LENGTH 280 MM, RX ONLY, Non Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix Srl
30 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2019
ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Prismaflex Control Unit, software versions below 7.21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Nov 13, 2019
SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemoglobins by agarose…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Helena Laboratories, Corp.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Hitachi Scenaria Whole-body X-ray CT System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
StemPro¿ MSC SFM CTS"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex-Morrisville
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Grab n Go Opti system is an integrated delivery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western / Scott Fetzer Company
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2019
Rastelli Bros., Inc. Retira Productos De Carne De Res Debido A Una Posible Contaminacin Con Materia Extraa
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rastelli
USDA FSIS
Reported Nov 6, 2019
TherMax Blood Warmer Unit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2019
CardioLab/ComboLab Recording Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pajunk GmbH
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Bulk Dry Apricot in clear plastic bags inside brown cardboard box and Swan brand Dry Appricot & Keshav brand Dry…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peekay International, Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2019
GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard package. 24 packages per master case. The following codes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rong Shing Trading Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2019
Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rong Shing Trading NY Inc.
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.