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 Apr 9, 2014
Weck Vista Universal Laparoscopic Port, Size 5/10mm x 100mm, Catalog No. 405910, Weck Vista Universal Laparoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 9, 2014
Tom Yom Soup, 24 oz. plastic cups, packed 6 cups\cardboard case, and labeled in part ***Manufactured by Whole Foods…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market Mid-Atlantic Kitchen
FDA (openFDA food enforcement)
Reported Apr 2, 2014
AMS BUN UREA NITROGEN For the In vitro quantitative determination of Urea Nitrogen in serum Quantitative determination…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMS Diagnostics, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
Chicken Soup for the Soul Thai-Style Chicken Broth, 32 oz. (2 lb., 907 g. paperboard carton. Distributed by Chicken…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chicken Soup For The Soul Food
FDA (openFDA food enforcement)
Reported Apr 2, 2014
Italian blend Salad (Romaine Lettuce and Radicchio) packaged under the following brand names: Dole Italian Blend, (UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Apr 2, 2014
Sausage & Egg English Muffin, Good and Fresh brand, 4.1 oz, packaged in clear plastic wrap. UPC 855173005204.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flying Food Group LLC
FDA (openFDA food enforcement)
Reported Apr 2, 2014
HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thoratec Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Velocity Medical Solutions, LLC
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Reusable Clip Applier Manufactured by AtriCure, Inc., 6217 Centre Park Drive, West Chester, OH 45069. The Reusable Clip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atricure Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens, FL 33410 USA 1-800-342-5454***EDAZ , EDAZx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Halogen Lamp component in RetCam 3 System - Clarity Medical Systems, Inc; Pleasanton, CA. General ophthalmic imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clarity Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for radiation therapy treatments of malignant neoplastics…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. The HeartStart FR3 is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems North America Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Hydroxyprogesterone Caproate 250mg/ml in Sesame Oil, 1 ml injectable solution, in 3 ml single dose syringes; a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RX South LLC dba RX3 Pharmacy
FDA (openFDA drug enforcement)
Reported Mar 26, 2014
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Navigator Surgical Kit Product Usage: Molded plastic tray used in holding various dental instruments for autoclave…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
RetCam 3, RetCam Portable and RetCam Shuttle; manufactured by Clarity Medical Systems, Inc.; Pleasanton, CA 94588.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clarity Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, Innova 3131IQ;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version 5.4, 5.5, or 5.6 with the Automatic-View-On-…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mckesson Technologies Inc.
FDA (openFDA device enforcement)
Reported Mar 12, 2014
Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes, 100 units/mL, 3 mL fill in a 12 mL…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medefil Incorporated
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.