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 48,124 notices were distributed nationwide, so they reach Maryland too — those are in the archive.

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)

Medical devices

Reported Sep 24, 2014

Ultraslim. These include all products labeled as UltraSlim, Luxurian, BioSlim Lipo, Cellulize, Slim 'n Trim, UltraRed,…

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

Advanced Photonic Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.

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

Amerx Health Care Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Food

Reported Sep 24, 2014

Price Chopper Orange Juice; 100% Pure ORANGE JUICE FROM CONCENTRATE; DISTRIBUTED BY THE PRICE CHOPPER, INC.,…

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

Dean Foods, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 24, 2014

Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674,…

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

GF Health Products, Inc./d.b.a.Basic American Metal Products

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

TRx Vertical Positioner, Classification Name: Wheelchair Component - Power Positioning System.

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

Motion Concepts

FDA (openFDA device enforcement)

Food

Reported Sep 24, 2014

Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…

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

Swanson Health Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2014

The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for the direct detection of…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves, REF 500-LB, Sterile. When left in place for five (5)…

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

Catheter Connections, Inc.

FDA (openFDA device enforcement)

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Other states

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.