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.
1,582 stored notices name Hawaii, reported between Jun 27, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.
Reported Mar 14, 2018
Flexible Shaft hip and anatomical shoulder instrument used for preparation of bone in Trauma, Hip and Shoulder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Agility with Integrity R3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Limited
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381
High riskUsing this product could cause serious injury, illness or death — stop using it now.Seggiano USA Inc.
FDA (openFDA food enforcement)
Reported Mar 7, 2018
Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2018
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported…
High riskUsing this product could cause serious injury, illness or death — stop using it now.J F C International Inc.
FDA (openFDA food enforcement)
Reported Feb 7, 2018
IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT; 100 ml and 250 ml sizes; UPC 100 ml - 7 93232 54200 3; UPC 250 ml - 7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Manicaretti Inc.
FDA (openFDA food enforcement)
Reported Feb 7, 2018
Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Ottogi Rice Cake Soup, 6.4oz. UPC 6 45175 89093 52; Item Number 29409101; Ingredients: 1. Rice Cake: Rice Water, Salt,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ottogi America Inc.
FDA (openFDA food enforcement)
Reported Jan 24, 2018
ACCOLADE SR Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
23 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2018
Hanryosued (F. Dashi Anchovy) 1.5kg x pack/carton UPC 826546102745, 826546102378
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hong Chang Corporation
FDA (openFDA food enforcement)
Reported Jan 24, 2018
Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2018
Certitude Delivery System and any associated Multipacks Models - 9600CT20A, 9600CT23A, 9600CT26A, 9600CT29A Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jan 17, 2018
UNIVERSAL FLEX2 BREATHING CIRCUIT, Item Numbers: D460-6133Z, D390-6121Z, D390-6121Z, D495-61Z, DF4116-6121Z, D466-61Z,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Systems Corp. dba Ambu, Inc.
FDA (openFDA device enforcement)
Reported Jan 17, 2018
Mobile Mini C-arm system Part # 1000-0001. Intended to provide the physician with general fluoroscopic visualization of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthoscan, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2017
Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 20, 2017
UniCel DxH800, Part Numbers: 629029 and B24802, automated hematology analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 20, 2017
ABL800 analyzer with FLEXQ module. Device intended for in vitro testing of samples of whole blood for the parameters…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Dec 13, 2017
TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM), Catalog Number 221261 Trypticase Soy Agar with 5% or 10% Sheep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 6, 2017
Casa Sanchez Foods, Real Guacamole; Net Wt. 9 oz.. (255 g), 1/2 gallon UPC: 0 78732 00412 2; 78732 00431-3 ;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.FANTE, Inc., dba Casa Sanchez Foods
1 more product in this recall
FDA (openFDA food 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.