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.

4,062 stored notices name Maryland, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Maryland too — those are in the archive.

Food

Reported Oct 29, 2014

next by Nature brand DARK CHOCOLATE CHERRIES, NET WT. 3 Oz (85 g), UPC 817582252006 --- Produced by Tropical Valley…

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

Tropical Valley Foods, Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported Oct 24, 2014

New Jersey Firm Recalls Salad with Chicken Due To Misbranding and Undeclared Allergen

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

Taylor Farms New Jersey, Inc.

USDA FSIS

Medical devices

Reported Oct 22, 2014

Omni Micro-electrode/reference electrode for cobas b221 analyzer. The Roche Diagnostics Omni S Analyzer is a fully…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2014

Stryker T2 Tibia System Nail Insertion Sleeve, Elastic, Sterile, a) REF 1806-1406S, SPI 08-11 and b) REF 1806-1407S,…

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

Stryker Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 15, 2014

ArjoHuntleigh Contoura C1000 series beds are designed to accommodate patients weighing up to 990 lbs. (450 kg). Model…

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

Arjo Hospital Equipment AB

FDA (openFDA device enforcement)

Medical devices

Reported Oct 15, 2014

RECLAIM Distal Reamer Extension Non Sterile REF 2975-00-500 Intended as an attachment device to the distal reamers to…

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

DePuy Orthopaedics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 15, 2014

Hostess Frosted Bagged Donettes, 11.25 oz

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

Hostess Brands LLC

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 15, 2014

Mars Chocolate North America Milk Chocolate M & M's Net Wt. 3.40 oz packed in a brown, 3 inch x 6.5 inch cardboard box…

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

Mars Chocolate North America

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 15, 2014

McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition,…

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

Mckesson Information Solutions LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 15, 2014

Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS:…

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

Nemschoff Chairs, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 15, 2014

Protocol 10% NBF Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological…

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

Richard-Allan Scientific Company

6 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 8, 2014

Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd.

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

Eugene Oregon, Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 8, 2014

GE Healthcare Precision 500D, Classical R&F System. Product Usage: The Precision 500D R&F X-ray System is intended…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior…

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

Instrumed International, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2014

Verigene BC-GP Kit (Catalog number 20-005-018); 1) 20 Verigene BC-GP Test Cartridges; are qualitative multiplexed in…

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

Nanosphere, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2014

The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2014

Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 1, 2014

Natural Blue Diamond Almonds Artisan Nut-Thins crafted with brown rice, almonds & Chia Seeds Wheat & Gluten free Net…

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

Blue Diamond Growers

FDA (openFDA food enforcement)

Medical devices

Reported Oct 1, 2014

0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion…

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

Centurion Medical Products Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN), performed using the sample-to-result Verigene…

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

Nanosphere, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

VITROS Immunodiagnostic Products Anti-HCV Reagent Pack for in vitro qualitative detection of immunoglobulin G antibody…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a polyester [poly(ethylene terephtalate)]…

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

Peters Surgical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

No packaging. The device is a computed tomography scanner. Intended to provide corss sectional images of the human body…

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455

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

Vidacare Corporation

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.