All recall categories

Recalls distributed in Hawaii

These notices name Hawaii 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.

1,551 stored notices name Hawaii, reported between Jun 27, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.

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

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)

Drugs

Reported Sep 24, 2014

Warfarin Sodium Tablets, USP Crystalline, 2 mg, 100 and 1000 Tablet Bottles, Rx Only. Mfd. by: Taro Pharmaceutical…

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

Taro Pharmaceuticals U.S.A., Inc.

FDA (openFDA drug 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

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)

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)

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

Tiny Isle Chocolate Truffles: Gluten Free, Raw, Vegan; Sold in 4 pack box - 4 oz: Flavors: Sea Salt, Coconut, Macadamia…

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

Florimont, Inc.

13 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 3, 2014

ORGANIC TRADITIONS SPROUTED CHIA SEED POWDER NET WT. 8 oz. and 16 oz., UPC 854260006162, item number AHM616 and UPC…

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

Health Matters America Inc.

4 more products in this recall

FDA (openFDA food 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

The Thermedx Fluid Management System is designed to provide irrigation fluids to irrigate, distend, and debride while…

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

Thermedx LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

GE Healthcare, Discovery XR656P/N 5374989/5397837 is intended to generate digital radiographic images of the skull,…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and device controller for…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

TomoTherapy Treatment System, Model: Hi-Art, Catalog/Part Number: H-0000-0003, software versions 1.2.0, 1.2.1 and 1.2.2…

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

TomoTherapy Incorporated

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer

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

Zimmer, Inc.

15 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging

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

Biosound Esaote, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2014

Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…

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

Mckesson Medical Immaging

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.