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 May 29, 2019
EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 29, 2019
Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
75 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Vega White Headless Shrimp, 21/15 and 26/30 count size. Frozen block in plastic bag, 6 x 4 lbs. per master carton.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Union Fish Company
FDA (openFDA food enforcement)
Reported May 15, 2019
Dried whole elderberry, Oregon s Wild Harvest brand, packaged in metalized plastic bag, net wt. 4 oz or 1 lb. Each case…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oregons Wild Harvest Inc.
FDA (openFDA food enforcement)
Reported May 15, 2019
T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off…
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 May 8, 2019
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 8, 2019
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported May 8, 2019
Trader Joe's Saucy Scallops with Mushrooms, NET Wt. 16 oz. (1 LB) 454 g UPC 0093 0390 24 units per case Product of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frial SAS
FDA (openFDA food enforcement)
Reported May 8, 2019
cobas e 801 immunoassay analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported May 1, 2019
Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled as the following kits: 1. AT-1 sets and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2019
FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cordis Corporation
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
25 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical unit for endoscopic polypectomy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2019
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 10, 2019
McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cypress Medical Products LLC
FDA (openFDA device enforcement)
Reported Apr 10, 2019
Maika'i Sweet Honey Nut Snack Mix, Honey Sesame Sticks, Almonds, Pumpkin Seeds, Peanuts, Pistachios & Pecans. NET WT. 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Newport Ingredients
FDA (openFDA food enforcement)
Reported Apr 3, 2019
Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous Autotransfusion System) is indicated for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries Inc.
FDA (openFDA device enforcement)
Reported Mar 27, 2019
Ne-Mo's Chocolate Cake Square with Cream Cheese Icing, item 104; Net Wt. 3 oz. Case UPC: 2007606401046 4; Display pk 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horizon Food Group
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 20, 2019
VITROS Chemistry Products Na+ Slides, Catalog Number 8379034 For in vitro diagnostic use only. VITROS Na+ Slides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Mar 20, 2019
Ossur Skull Pin, Sterile Titanium Pin, Part/Description: 516TS/ Skull Pin 2-1/4in TI Sterl 1PK; 516V2S/ Skull Pin 3in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
7 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.