All recall categories

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.

Medical devices

Reported Sep 17, 2014

CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/ Hysterosalpingography.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

CARESCAPE Respiratory Modules E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE; the Airway Gas Option N-CAiO and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Sep 17, 2014

Grace Classic Coconut Milk Net 13.5 FL OZ (US) (400 mL) PRODUCT OF THAILAND Packed for: GraceKennedy Limited, 73…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Grace Foods (USA) Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2014

Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Life Force

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012. Used use in conjunction with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Cardiovascular Surgery-the Heart Valve Division

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

Prime Care ¿ Transcend Mattress, Prime Care ¿ Transcend Perimeter Mattress, Prime Care ¿ Transcend Advanced Mattress,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Primus Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

Stryker Aria Implant Inserter, REF 48758500, This instrument is part of the Aria product brand. It is used for Implant…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Spine

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2014

Hitachi Echelon Oval MRI system is a diagnostic imaging device (one unit per package) and is intended to provide the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2014

Brown carob powder packed in a plastic heat sealed 16oz. bag, labeled in part "Live Superfoods Carob Powder***NET WT 16…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Live Superfoods

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2014

EN MENTOR Round High Profile Single Use Saline Breast Implant Sizer Single Use Saline Breast Implant Sizer REF…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mentor Texas, LP.

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2014

Organic Carob Powder; Certified Organic, Product of Italy. Store in Cool, Dark place. Packaged in 16 oz., 5 lb., 20 lb…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

River Canyon Retreat

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2014

Roche cobas IT 1000 Product Usage: Intended Use: An electronic device intended to store, retrieve, and process…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2014

Organic Carob Powder, 1 lb., 20 lb., and 55 lb. bags Expiry date: 6/5/2015, UPC Code 803813-04429-8

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sunfood Superfoods

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2014

PERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2014

Rising Moon Organics Butternut Squash Ravioli, Organic, Vegetarian & Delicious; Keep Frozen; Net Wt. 8 oz. UPC:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carmel Food Group, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2014

CollectEVAC, Sterile device with tubing and adaptor for use with ACMI and STORZ/Wolf resectoscopes. Part number…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Civco Medical Instruments Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2014

CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a Tyvek-film sterilizable outer package and is…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2014

Cordis EMPIRA NC RX PTCA Dilatation Catheter

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cordis Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2014

McCormick Ground Oregano in 0.75 oz plastic bottle. UPC NUMBER: 52100003566 (as seen on label: 0-523561-6) MCCORMICK…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

McCormick & Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2014

Verigene CYP2C19 Nucleic Acid Test (CYP2C19 Test). Each CYP2C19 kit consists of 20 Verigene CYP2C19 Nucleic Acid Test…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Nanosphere, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Sep 3, 2014

Midazolam HCl 2 mg/ml in 0.9% Sodium Chloride in 30 mL PVC Vial, Rx Only. Pharmakon Pharmaceuticals, Inc., 14450 Getz…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Pharmakon Pharmaceuticals

3 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Sep 3, 2014

Shoprite Spring Water Net 1 GAL (120 Fl Oz.) 3.78L Distributed by Wakefern Food Corp Elizabeth, NJ Made in USA UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Readington Farms Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2014

4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy, LDS 15mm Conn Pediatric Endotracheal Intubation Kit

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Smiths Medical ASD, Inc.

5 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.