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 Dec 19, 2012
Novocastra Ready-to-Use Mouse Monoclonal Antibody Terminal Deoxynuceotidyl Transferase Staining Reagent; an in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Dec 19, 2012
Baby Quasar (LAB-001-D, BQ101) and Baby Quasar Pink (LAB-046-A BQ101-P) are infrared LED lamps that are labeled in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quasar Bio-Tech, Inc. dba Silver Bay LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Cobas 8000 Modular Analyzer Series, Model/Catalog/Part Number: 05641489001. The Cobas 8000 is a fully automated system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Echo Bi-Metric Press-Fit Stems/Echo Bi-Metric 11mm x 135mm Collarless Porous Stem (Orthopedic Implant) Indications: 1)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Ground Hot Pepper Chillies, 5 oz. plastic jars, 24 jars/case; jars labeled in part ***Imported and distributed by Nina…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ernimich, Inc. (dba Nina International, Inc.)
FDA (openFDA food enforcement)
Reported Dec 5, 2012
IO FiX X-Post Reamer, Extremity Medical, www.extremitymedical.com; Customer Service: 888.499.0079 The X-Post Reamer is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Jimmy Dean French Toast & Sausage Sandwich, Net Wt 3.9 oz (110g); a food service individually butcher paper wrapped,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hillshire Brands Company
FDA (openFDA food enforcement)
Reported Dec 5, 2012
The brand name is MRidium Series 1000 MR Infusion Sets, Type 1058 MR IV Extension Set, Lot Code LBG001. The generic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Iradimed Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
bioMerieux BacT/ALERT Control Module, catalog number 210147, Clinical instrument The product is most commonly used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
31 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
INTRABEAM Balloon Applicator Set; 3.0 cm, Carl Zeiss Meditec AG, Oberkochen, Germany INTRABEAM System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
IO Fix IntraOsseous Fixation System; Extremity Medical. www.extremitymedical.com; Customer Service: 888.499.0079. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Nov 28, 2012
IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innovative Magnetic Resonance Imaging Systems Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent Cartridge (K4071) The THEO method is an in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal scalp circular (spiral) electrode and applicator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Signs Devices, a GE Healthcare Company
FDA (openFDA device enforcement)
Reported Nov 21, 2012
PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dako North America Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
Select Medical Products Vinyl Powder-Free Exam Gloves, Medium Model # 6370 and Large Model # 6371, 100 per box; 10…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gulf South Medical Supply Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 (List Number 06F12-09; Lot Number 071039) Cliniqa Liquid…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clinical Diagnostic Solutions
4 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.